摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(+)-2-蒈烯 | 4497-92-1

中文名称
(+)-2-蒈烯
中文别名
蒈烯;(1S)-3,7,7-三甲基二环[4.1.0]庚-2-烯;2-蒈烯
英文名称
2-carene
英文别名
δ-2-carene;(+)-Δ2-carene;2-δ-carene;(+)-2-Carene;(1S,6R)-3,7,7-trimethylbicyclo[4.1.0]hept-2-ene
(+)-2-蒈烯化学式
CAS
4497-92-1
化学式
C10H16
mdl
——
分子量
136.237
InChiKey
IBVJWOMJGCHRRW-BDAKNGLRSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    25°C (estimate)
  • 沸点:
    167-168 °C(lit.)
  • 密度:
    0.862 g/mL at 25 °C(lit.)
  • 闪点:
    101 °F
  • LogP:
    4.321 (est)
  • 稳定性/保质期:

    在常温常压下,该物质是稳定的但易燃,并且具有刺激性。请避免吸入其蒸汽,同时不要让其接触到眼睛或皮肤。

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

安全信息

  • 危险品标志:
    Xi
  • 危险类别码:
    R10
  • 危险品运输编号:
    UN 3295 3/PG 3
  • 海关编码:
    2902199090
  • 安全说明:
    S16,S26,S36/37/39,S45
  • WGK Germany:
    3
  • 储存条件:
    请将药品存放在避光、通风干燥的地方,并密封保存。

SDS

SDS:1e3799427da304f3ee23edffe763044c
查看

SECTION 1: Identification of the substance/mixture and of the company/undertaking
Product identifiers
Product name : (+)-2-Carene
REACH No. : A registration number is not available for this substance as the substance
or its uses are exempted from registration, the annual tonnage does not
require a registration or the registration is envisaged for a later
registration deadline.
CAS-No. : 4497-92-1


SECTION 2: Hazards identification
Classification of the substance or mixture
Classification according to Regulation (EC) No 1272/2008
Flammable liquids (Category 3), H226
For the full text of the H-Statements mentioned in this Section, see Section 16.
Classification according to EU Directives 67/548/EEC or 1999/45/EC
R10
For the full text of the R-phrases mentioned in this Section, see Section 16.
Label elements
Labelling according Regulation (EC) No 1272/2008
Pictogram
Signal word Warning
Hazard statement(s)
Flammable liquid and vapour.
Precautionary statement(s) none
Supplemental Hazard none
Statements
Other hazards - none

SECTION 3: Composition/information on ingredients
Substances
Formula : C10H16
Molecular Weight : 136,23 g/mol
CAS-No. : 4497-92-1
EC-No. : 224-792-4
No components need to be disclosed according to the applicable regulations.
For the full text of the H-Statements and R-Phrases mentioned in this Section, see Section 16

SECTION 4: First aid measures
Description of first aid measures
General advice
Consult a physician. Show this safety data sheet to the doctor in attendance.
If inhaled
If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician.
In case of skin contact
Wash off with soap and plenty of water. Consult a physician.
In case of eye contact
Flush eyes with water as a precaution.
If swallowed
Do NOT induce vomiting. Never give anything by mouth to an unconscious person. Rinse mouth with
water. Consult a physician.
Most important symptoms and effects, both acute and delayed
The most important known symptoms and effects are described in the labelling (see section 2.2) and/or in
section 11
Indication of any immediate medical attention and special treatment needed
no data available

SECTION 5: Firefighting measures
Extinguishing media
Suitable extinguishing media
For small (incipient) fires, use media such as "alcohol" foam, dry chemical, or carbon dioxide. For large
fires, apply water from as far as possible. Use very large quantities (flooding) of water applied as a mist or
spray; solid streams of water may be ineffective. Cool all affected containers with flooding quantities of
water.
Special hazards arising from the substance or mixture
Carbon oxides
Advice for firefighters
Wear self contained breathing apparatus for fire fighting if necessary.
Further information
Use water spray to cool unopened containers.

SECTION 6: Accidental release measures
Personal precautions, protective equipment and emergency procedures
Avoid breathing vapours, mist or gas. Remove all sources of ignition. Beware of vapours accumulating to
form explosive concentrations. Vapours can accumulate in low areas.
For personal protection see section 8.
Environmental precautions
Prevent further leakage or spillage if safe to do so. Do not let product enter drains.
Methods and materials for containment and cleaning up
Contain spillage, and then collect with an electrically protected vacuum cleaner or by wet-brushing and
place in container for disposal according to local regulations (see section 13).
Reference to other sections
For disposal see section 13.

SECTION 7: Handling and storage
Precautions for safe handling
Avoid inhalation of vapour or mist.
Keep away from sources of ignition - No smoking.Take measures to prevent the build up of electrostatic
charge.
For precautions see section 2.2.
Conditions for safe storage, including any incompatibilities
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Containers which are
opened must be carefully resealed and kept upright to prevent leakage.
Specific end use(s)
Apart from the uses mentioned in section 1.2 no other specific uses are stipulated

SECTION 8: Exposure controls/personal protection
Control parameters
Components with workplace control parameters
Exposure controls
Appropriate engineering controls
Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and
at the end of workday.
Personal protective equipment
Eye/face protection
Face shield and safety glasses Use equipment for eye protection tested and approved under
appropriate government standards such as NIOSH (US) or EN 166(EU).
Skin protection
Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique
(without touching glove's outer surface) to avoid skin contact with this product. Dispose of
contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.
The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and
the standard EN 374 derived from it.
Full contact
Material: Nitrile rubber
Minimum layer thickness: 0,4 mm
Break through time: 480 min
Splash contact
Material: Nature latex/chloroprene
Minimum layer thickness: 0,6 mm
Break through time: 30 min
test method: EN374
If used in solution, or mixed with other substances, and under conditions which differ from EN 374,
contact the supplier of the CE approved gloves. This recommendation is advisory only and must
be evaluated by an industrial hygienist and safety officer familiar with the specific situation of
anticipated use by our customers. It should not be construed as offering an approval for any
specific use scenario.
Body Protection
impervious clothing, Flame retardant antistatic protective clothing, The type of protective
equipment must be selected according to the concentration and amount of the dangerous
substance at the specific workplace.
Respiratory protection
Where risk assessment shows air-purifying respirators are appropriate use a full-face respirator
with multi-purpose combination (US) or type ABEK (EN 14387) respirator cartridges as a backup
to engineering controls. If the respirator is the sole means of protection, use a full-face supplied air
respirator. Use respirators and components tested and approved under appropriate government
standards such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Prevent further leakage or spillage if safe to do so. Do not let product enter drains.

SECTION 9: Physical and chemical properties
Information on basic physical and chemical properties
a) Appearance Form: clear, liquid
Colour: colourless
b) Odour no data available
c) Odour Threshold no data available
d) pH no data available
e) Melting point/freezing no data available
point
f) Initial boiling point and 167 - 168 °C
boiling range
g) Flash point 38 °C - closed cup
h) Evapouration rate no data available
i) Flammability (solid, gas) no data available
j) Upper/lower no data available
flammability or
explosive limits
k) Vapour pressure no data available
l) Vapour density no data available
m) Relative density 0,862 g/mL at 25 °C
n) Water solubility no data available
o) Partition coefficient: n- no data available
octanol/water
p) Auto-ignition no data available
temperature
q) Decomposition no data available
temperature
r) Viscosity no data available
s) Explosive properties no data available
t) Oxidizing properties no data available
Other safety information
no data available

SECTION 10: Stability and reactivity
Reactivity
no data available
Chemical stability
Stable under recommended storage conditions.
Possibility of hazardous reactions
no data available
Conditions to avoid
Heat, flames and sparks.
Incompatible materials
Strong oxidizing agents
Hazardous decomposition products
Other decomposition products - no data available
In the event of fire: see section 5

SECTION 11: Toxicological information
Information on toxicological effects
Acute toxicity
no data available
Skin corrosion/irritation
no data available
Serious eye damage/eye irritation
no data available
Respiratory or skin sensitisation
no data available
Germ cell mutagenicity
no data available
Carcinogenicity
IARC: No component of this product present at levels greater than or equal to 0.1% is identified as
probable, possible or confirmed human carcinogen by IARC.
Reproductive toxicity
no data available
Specific target organ toxicity - single exposure
no data available
Specific target organ toxicity - repeated exposure
no data available
Aspiration hazard
no data available
Additional Information
RTECS: Not available
To the best of our knowledge, the chemical, physical, and toxicological properties have not been
thoroughly investigated.

SECTION 12: Ecological information
Toxicity
no data available
Persistence and degradability
no data available
Bioaccumulative potential
no data available
Mobility in soil
no data available
Results of PBT and vPvB assessment
PBT/vPvB assessment not available as chemical safety assessment not required/not conducted
Other adverse effects
no data available

SECTION 13: Disposal considerations
Waste treatment methods
Product
Burn in a chemical incinerator equipped with an afterburner and scrubber but exert extra care in igniting
as this material is highly flammable. Offer surplus and non-recyclable solutions to a licensed disposal
company. Contact a licensed professional waste disposal service to dispose of this material.
Contaminated packaging
Dispose of as unused product.

SECTION 14: Transport information
UN number
ADR/RID: 2319 IMDG: 2319 IATA: 2319
UN proper shipping name
ADR/RID: TERPENE HYDROCARBONS, N.O.S.
IMDG: TERPENE HYDROCARBONS, N.O.S.
IATA: Terpene hydrocarbons, n.o.s.
Transport hazard class(es)
ADR/RID: 3 IMDG: 3 IATA: 3
Packaging group
ADR/RID: III IMDG: III IATA: III
Environmental hazards
ADR/RID: no IMDG Marine pollutant: no IATA: no
Special precautions for user
no data available

SECTION 15: Regulatory information
This safety datasheet complies with the requirements of Regulation (EC) No. 1907/2006.
Safety, health and environmental regulations/legislation specific for the substance or mixture
no data available
Chemical Safety Assessment
For this product a chemical safety assessment was not carried out


SECTION 16 - ADDITIONAL INFORMATION
N/A



制备方法与用途

生产方法

2-蒈烯3-蒈烯是广泛存在于植物中的一种化合物,主要来源于芬兰松节油和印度松节油等。它们可以通过分馏松节油而获得。

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Enantioselective Baeyer–Villiger Oxidation Catalyzed by Palladium(II) Complexes with Chiral <i>P,N</i>-Ligands
    作者:Andrei V. Malkov、Frédéric Friscourt、Mark Bell、Martin E. Swarbrick、Pavel Kočovský
    DOI:10.1021/jo800246g
    日期:2008.6.1
    Asymmetric Baeyer–Villiger reaction of symmetrical cyclobutanones 1a−j with urea−hydrogen peroxide (UHP) can be catalyzed by a complex of Pd(II) and the new terpene-derived P,N-ligand 7. The resulting lactones 2a−j were obtained in high yields and with good enantioselectivity (≤81% ee).
    对称cyclobutanones的不对称拜尔-维利格反应1A - Ĵ与-过氧化氢(UHP)可以通过一个复杂的Pd(II)和新的萜烯衍生的催化P,ñ -配体7。得到的内酯2a - j以高收率和良好的对映选择性(≤81%ee)获得。
  • Development of Enantiospecific Coupling of Secondary and Tertiary Boronic Esters with Aromatic Compounds
    作者:Marcin Odachowski、Amadeu Bonet、Stephanie Essafi、Philip Conti-Ramsden、Jeremy N. Harvey、Daniele Leonori、Varinder K. Aggarwal
    DOI:10.1021/jacs.6b03963
    日期:2016.8.3
    functional groups (esters, azides, nitriles, alcohols, and ethers). The reaction also worked well with other electron-rich heteroaromatics and 6-membered ring aromatics provided they had donor groups in the meta position. Conditions were also found under which the B(pin)- moiety could be retained in the product, ortho to the boron substituent. This protocol, which created a new C(sp2)–C(sp3) and an adjacent
    硼酸酯与 sp2 亲电试剂的立体有择交叉偶联(Suzuki-Miyaura 反应)是合成中长期存在的问题,但在使用催化的特定情况下已经取得了进展。然而,目前无法实现与叔硼酸酯的相关偶联。为了解决这一普遍问题,我们专注于利用芳基硼酸酯之间形成的硼酸盐络合物的反应性的替代方法。我们推断,随后添加氧化剂或亲电子试剂会分别从芳环中去除电子或以 Friedel-Crafts 型方式反应,产生阳离子物质,这将引发取代基的 1,2-迁移,创建新的 C-C 键。消除(在前一种情况下,在进一步氧化之前)将导致重新芳构化,从而立体特异性地产生偶联产物。最初的工作是用 2-furyllithium 检查的。尽管测试的氧化剂不成功,但亲电试剂,特别是 NBS,使得偶联反应能够以良好的收率与范围广泛的仲和叔硼酸酯发生偶联反应,具有不同的空间需求和官能团(酯、叠氮化物、腈、醇和醚) )。该反应也适用于其他富电子杂芳烃
  • Substrate-Induced Diastereoselectivity in the Dimethyldioxirane Epoxidation of Simple Alkenes and Dienes
    作者:Amalia Asouti、Lazaros P. Hadjiarapoglou
    DOI:10.1055/s-2001-18751
    日期:——
    Various alkenes and dienes, such as (R)- or (S)-limonene 2, 2-carene 6, 3-carene 8, (R)-α-pinene 10, (S)-α-pinene 12, and endo-dicyclopentadiene 14 were transformed into the corresponding mono- and bis-epoxides by epoxidation with dimethyldioxirane (as an acetone solution). The selectivity observed in these epoxidations is explained by the assumption of hydrogen bonding between bridge protons and the dioxirane.
    各种烯烃和二烯烃,例如(R)-或(S)-柠檬烯2、2-蒈烯6、3-蒈烯8、(R)-α-蒎烯10、(S)-α-蒎烯12以及endo-二环戊二烯14,通过二甲基二氧杂环丙烷(以丙酮溶液形式)的环氧化反应,被转化为相应的单环氧和双环氧化合物。在这些环氧化过程中观察到的选择性可以通过桥连质子与二氧杂环丙烷之间氢键的假设来解释。
  • Syntheses of the Optically Active Terpene Hydroxyphenylselenides
    作者:Jacek Ścianowski、Mirosław Wełniak
    DOI:10.1080/10426500902947682
    日期:2009.6.23
    The optically active hydroxyphenylselenides derived from the p-menthane, carane, and pinane systems have been obtained. Two methods of hydroxyphenylselenides synthesis have been compared. The first method is based on the reaction of alkenes with N-(phenylseleno)succinimide in the presence of water, and the second from epoxides as a result of the reaction with sodium benzeneselenolate. The influence
    已经获得了衍生自对薄荷烷、卡拉烷和蒎烷体系的旋光羟基苯化物。已经比较了羟苯基化物的两种合成方法。第一种方法基于烯烃与 N-(苯基基)琥珀酰亚胺存在下的反应,第二种方法是与苯硒酸反应产生的环氧化物。已经证明了基材结构对所得产品组成的影响。
  • Relative and Absolute Structure Assignments of Alkenes Using Crystalline Osmate Derivatives for X-ray Analysis
    作者:Alexander S. Burns、Charles Dooley、Paul R. Carlson、Joseph W. Ziller、Scott D. Rychnovsky
    DOI:10.1021/acs.orglett.9b04133
    日期:2019.12.20
    stable crystalline adducts with alkenes. The structure of liquid alkenes can be determined through the X-ray analysis of these derivatives. Osmium, a heavy atom, facilitates the crystallographic analysis and the determination of the absolute configuration using common Mo X-ray sources. The utility of this method for assigning structures and absolute configurations was demonstrated on a number of unsaturated
    四氧化和TMEDA与烯烃形成稳定的结晶加合物。液态烯烃的结构可以通过对这些衍生物的X射线分析来确定。common是重原子,可使用常见的Mo X射线源促进晶体学分析和确定绝对构型。在许多不饱和底物上证明了该方法用于分配结构和绝对构型的效用,这些不饱和底物包括简单的烯烃,烯酮,烯醇醚和甲硅烷基烯醇醚。
查看更多

同类化合物

(5β,6α,8α,10α,13α)-6-羟基-15-氧代黄-9(11),16-二烯-18-油酸 (3S,3aR,8aR)-3,8a-二羟基-5-异丙基-3,8-二甲基-2,3,3a,4,5,8a-六氢-1H-天青-6-酮 (2Z)-2-(羟甲基)丁-2-烯酸乙酯 (2S,4aR,6aR,7R,9S,10aS,10bR)-甲基9-(苯甲酰氧基)-2-(呋喃-3-基)-十二烷基-6a,10b-二甲基-4,10-dioxo-1H-苯并[f]异亚甲基-7-羧酸盐 (1aR,4E,7aS,8R,10aS,10bS)-8-[((二甲基氨基)甲基]-2,3,6,7,7a,8,10a,10b-八氢-1a,5-二甲基-氧杂壬酸[9,10]环癸[1,2-b]呋喃-9(1aH)-酮 (+)顺式,反式-脱落酸-d6 龙舌兰皂苷乙酯 龙脑香醇酮 龙脑烯醛 龙脑7-O-[Β-D-呋喃芹菜糖基-(1→6)]-Β-D-吡喃葡萄糖苷 龙牙楤木皂甙VII 龙吉甙元 齿孔醇 齐墩果醛 齐墩果酸苄酯 齐墩果酸甲酯 齐墩果酸溴乙酯 齐墩果酸二甲胺基乙酯 齐墩果酸乙酯 齐墩果酸3-O-alpha-L-吡喃鼠李糖基(1-3)-beta-D-吡喃木糖基(1-3)-alpha-L-吡喃鼠李糖基(1-2)-alpha-L-阿拉伯糖吡喃糖苷 齐墩果酸 beta-D-葡萄糖酯 齐墩果酸 beta-D-吡喃葡萄糖基酯 齐墩果酸 3-乙酸酯 齐墩果酸 3-O-beta-D-葡吡喃糖基 (1→2)-alpha-L-吡喃阿拉伯糖苷 齐墩果酸 齐墩果-12-烯-3b,6b-二醇 齐墩果-12-烯-3,24-二醇 齐墩果-12-烯-3,21,23-三醇,(3b,4b,21a)-(9CI) 齐墩果-12-烯-3,21,23-三醇,(3b,4b,21a)-(9CI) 齐墩果-12-烯-3,11-二酮 齐墩果-12-烯-2α,3β,28-三醇 齐墩果-12-烯-29-酸,3,22-二羟基-11-羰基-,g-内酯,(3b,20b,22b)- 齐墩果-12-烯-28-酸,3-[(6-脱氧-4-O-b-D-吡喃木糖基-a-L-吡喃鼠李糖基)氧代]-,(3b)-(9CI) 齐墩果-12-烯-28-酸,3,7-二羰基-(9CI) 齐墩果-12-烯-28-酸,3,21,29-三羟基-,g-内酯,(3b,20b,21b)-(9CI) 鼠特灵 鼠尾草酸醌 鼠尾草酸 鼠尾草酚酮 鼠尾草苦内脂 黑蚁素 黑蔓醇酯B 黑蔓醇酯A 黑蔓酮酯D 黑海常春藤皂苷A1 黑檀醇 黑果茜草萜 B 黑五味子酸 黏黴酮 黏帚霉酸