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9-溴-2-硝基芴 | 53172-79-5

中文名称
9-溴-2-硝基芴
中文别名
——
英文名称
9-bromo-2-nitro-fluorene
英文别名
9-Brom-2-nitro-fluoren;(+/-)-9-Brom-2-nitro-fluoren;2-Nitro-9-brom-fluoren;9-Bromo-2-nitrofluoren;9-Brom-2-nitrofluoren;9-Bromo-2-Nitrofluorene;9-bromo-2-nitro-9H-fluorene
9-溴-2-硝基芴化学式
CAS
53172-79-5
化学式
C13H8BrNO2
mdl
——
分子量
290.116
InChiKey
MQMLOKJKGOPCKW-UHFFFAOYSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    3.7
  • 重原子数:
    17
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    45.8
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2904909090

SDS

SDS:75fbb96700231ac0355ada9e0dc26191
查看

Section 1. IDENTIFICATION OF THE SUBSTANCE/MIXTURE
Product identifiers
Product name : 9-Bromo-2-nitrofluorene
CAS-No. : 53172-79-5
Relevant identified uses of the substance or mixture and uses advised against
Identified uses : Laboratory chemicals, Manufacture of substances



Section 2. HAZARDS IDENTIFICATION
Classification of the substance or mixture
Classification according to Regulation (EC) No 1272/2008 [EU-GHS/CLP]
Acute toxicity, Oral (Category 4)
Classification according to EU Directives 67/548/EEC or 1999/45/EC
Harmful if swallowed. Harmful to aquatic organisms, may cause long-term adverse effects in the aquatic
environment.
Label elements
Labelling according Regulation (EC) No 1272/2008 [CLP]
Pictogram
Signal word Warning
Hazard statement(s)
H302 Harmful if swallowed.
Precautionary statement(s) none
Supplemental Hazard none
Statements
According to European Directive 67/548/EEC as amended.
Hazard symbol(s)
R-phrase(s)
R22 Harmful if swallowed.
R52/53 Harmful to aquatic organisms, may cause long-term adverse effects in
the aquatic environment.
S-phrase(s)
S61 Avoid release to the environment. Refer to special instructions/ Safety
data sheets.
Other hazards - none

Section 3. COMPOSITION/INFORMATION ON INGREDIENTS
Substances
Formula : C13H8BrNO2
Molecular Weight : 290,11 g/mol
Component Concentration
9-Bromo-2-nitrofluorene
CAS-No. 53172-79-5 -

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
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
To the best of our knowledge, the chemical, physical, and toxicological properties have not been
thoroughly investigated.
Indication of any immediate medical attention and special treatment needed
no data available

Section 5. FIREFIGHTING MEASURES
Extinguishing media
Suitable extinguishing media
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Carbon oxides, nitrogen oxides (NOx), Hydrogen bromide gas
Advice for firefighters
Wear self contained breathing apparatus for fire fighting if necessary.
Further information
no data available

Section 6. ACCIDENTAL RELEASE MEASURES
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment. Avoid dust formation. Avoid breathing vapors, mist or gas. Ensure
adequate ventilation. Avoid breathing dust.
Environmental precautions
Prevent further leakage or spillage if safe to do so. Do not let product enter drains. Discharge into the
environment must be avoided.
Methods and materials for containment and cleaning up
Pick up and arrange disposal without creating dust. Sweep up and shovel. Keep in suitable, closed
containers for disposal.
Reference to other sections
For disposal see section 13.

Section 7. HANDLING AND STORAGE
Precautions for safe handling
Avoid contact with skin and eyes. Avoid formation of dust and aerosols.
Provide appropriate exhaust ventilation at places where dust is formed.Normal measures for preventive fire
protection.
Conditions for safe storage, including any incompatibilities
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
Specific end uses
no data available

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
Safety glasses with side-shields conforming to EN166 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.
Body Protection
Complete suit protecting against chemicals, The type of protective equipment must be selected
according to the concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection
For nuisance exposures use type P95 (US) or type P1 (EU EN 143) particle respirator.For higher
level protection use type OV/AG/P99 (US) or type ABEK-P2 (EU EN 143) respirator cartridges.
Use respirators and components tested and approved under appropriate government standards
such as NIOSH (US) or CEN (EU).

Section 9. PHYSICAL AND CHEMICAL PROPERTIES
Information on basic physical and chemical properties
a) Appearance Form: solid
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 no data available
boiling range
g) Flash point no data available
h) Evaporation 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 no data available
n) Water solubility no data available
o) Partition coefficient: n- no data available
octanol/water
p) Autoignition 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
no data available
Possibility of hazardous reactions
no data available
Conditions to avoid
no data available
Incompatible materials
Strong oxidizing agents
Hazardous decomposition products
Other decomposition products - no data available

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 sensitization
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
Potential health effects
Inhalation May be harmful if inhaled. May cause respiratory tract irritation.
Ingestion Harmful if swallowed.
Skin May be harmful if absorbed through skin. May cause skin irritation.
Eyes May cause eye irritation.
Signs and Symptoms of Exposure
To the best of our knowledge, the chemical, physical, and toxicological properties have not been
thoroughly investigated.
Additional Information
RTECS: Not available

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
no data available
Other adverse effects
Harmful to aquatic life.
no data available

Section 13. DISPOSAL CONSIDERATIONS
Waste treatment methods
Product
Offer surplus and non-recyclable solutions to a licensed disposal company. Contact a licensed
professional waste disposal service to dispose of this material. Dissolve or mix the material with a
combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber.
Contaminated packaging
Dispose of as unused product.

Section 14. TRANSPORT INFORMATION
UN number
ADR/RID: - IMDG: - IATA: -
UN proper shipping name
ADR/RID: Not dangerous goods
IMDG: Not dangerous goods
IATA: Not dangerous goods
Transport hazard class(es)
ADR/RID: - IMDG: - IATA: -
Packaging group
ADR/RID: - IMDG: - IATA: -
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
no data available

Section 16. OTHER INFORMATION
Further information
Copyright 2012 Co. LLC. License granted to make unlimited paper copies for internal use
only.
The above information is believed to be correct but does not purport to be all inclusive and shall be
used only as a guide. The information in this document is based on the present state of our knowledge
and is applicable to the product with regard to appropriate safety precautions. It does not represent any
guarantee of the properties of the product. Corporation and its Affiliates shall not be held
liable for any damage resulting from handling or from contact with the above product. See
and/or the reverse side of invoice or packing slip for additional terms and conditions of sale.

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

  • 作为反应物:
    描述:
    参考文献:
    名称:
    COMPOUNDS FOR CANCER RESEARCH. IV. FURTHER BIFLUORYL AND BIFLUORYLIDENE DERIVATIVES1
    摘要:
    DOI:
    10.1021/jo01155a023
  • 作为产物:
    描述:
    9-溴芴硝酸乙酸酐 作用下, 生成 9-溴-2-硝基芴
    参考文献:
    名称:
    381.在多环系统中的替代。第一部分:芴和9-溴芴的硝化
    摘要:
    DOI:
    10.1039/jr9350001607
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文献信息

  • Method for producing organic compounds by substituting halogen atoms
    申请人:MITSUI CHEMICALS, INC.
    公开号:EP1486479A1
    公开(公告)日:2004-12-15
    The invention pertains to a method in which a halogen atom of an organic compound is replaced with a group derived from a nucleophilic agent, at high yield and high efficiency, by the following method which includes a step of reacting the nucleophilic agent with an organic material having a halogen atom bonded to a carbon atom having four σ bonds, more specifically: a method for producing an organic compound having Q, the method including a step of reacting a compound represented by general formula (2) with an organic starting material having at least one halogen atom bonded to a carbon atom having four σ bonds so as to replace the halogen atom in the organic starting material with Q:         MQa     (2) (wherein M represents an alkali metal atom, an alkali earth metal atom, or a rare earth metal atom; Q represents a moiety of an inorganic acid or an active hydrogen compound derived by eliminating a proton, wherein Q is a halogen atom different from the halogen atom in the organic starting material having the halogen atom bonded to the carbon atom having the four σ bonds; and a represents an integer of 1 to 3) in the presence of a compound represented by general formula (1) (wherein Z- represents an anion derived by eliminating a proton from an inorganic acid or an active hydrogen compound; R2 is the same or different; R2 each independently represent a C1-C10 hydrocarbon group or two R2 on the same nitrogen atom may be bonded with each other to form a ring with the nitrogen atom).
    这项发明涉及一种方法,其中有机化合物中的卤素原子被来自亲核试剂的基团取代,且产率高效率高,通过以下方法实现,包括以下步骤:将亲核试剂与具有与碳原子形成四个σ键的卤素原子相结合的有机材料反应的步骤,更具体地说:一种用于生产具有Q的有机化合物的方法,包括以下步骤:将由通式(2)表示的化合物与至少一个卤素原子与碳原子形成四个σ键的有机起始材料反应,以将有机起始材料中的卤素原子替换为Q:         MQa     (2) (其中M代表碱金属原子、碱土金属原子或稀土金属原子;Q代表由消除质子衍生的无机酸或活性氢化合物的基团,其中Q是不同于有机起始材料中卤素原子的卤素原子,该卤素原子与具有四个σ键的碳原子相结合;a表示1到3的整数),在通式(1)表示的化合物的存在下 (其中Z-代表由无机酸或活性氢化合物中消除质子衍生的阴离子;R2相同或不同;R2各自独立地表示C1-C10烃基,或者两个R2在同一氮原子上可能与彼此结合形成与氮原子的环)。
  • ALIPHATIC CHEMISTRY OF FLUORENE:PART IV. PREPARATION AND ALKYLATION OF SOME SULPHIDES AND SULPHONES
    作者:P. M. G. Bavin
    DOI:10.1139/v60-129
    日期:1960.6.1
    The preparations are described of some 9-fluorenyl sulphides which have been oxidized with peracetic acid to the corresponding sulphones.9-Fluorenyl p-tolyl sulphone has been alkylated with a range of alkyl halides; other sulphones, including 2-nitro-9-fluorenyl p-tolyl sulphone, have been methylated.Methyl fluorene-9-carboxylate anion was reduced by p-toluenesulphonyl chloride to dimethyl 9,9′-difluorenyl-9
    描述了一些 9-芴基硫化物的制备方法,这些硫化物已被过乙酸氧化成相应的砜。9-芴基对甲苯基砜已被一系列烷基卤化物烷基化;其他砜,包括 2-硝基-9-芴基对甲苯基砜,已被甲基化。芴-9-羧酸甲酯阴离子被对甲苯磺酰氯还原为 9,9'-二芴基-9,9'-二甲酸二甲酯。
  • Method for producing organic compound by substituting halogen atoms
    申请人:Mitsui Chemicals, Inc.
    公开号:US20040256743A1
    公开(公告)日:2004-12-23
    A method for producing an organic compound having Q, the method including a step of reacting a compound represented by general formula (2) with an organic starting material having at least one halogen atom bonded to a carbon atom having four &sgr; bonds so as to replace the halogen atom in the organic starting material with Q: MQ a (2) wherein M, Q and a are defined in the presence of a compound represented by general formula (1) 1 wherein Z − and Rs are also defined.
    一种生产具有 Q 的有机化合物的方法,该方法包括以下步骤:将通式(2)代表的化合物与有机起始材料反应,该有机起始材料具有至少一个与具有四个&sgr;键的碳原子成键的卤原子,从而用 Q 取代有机起始材料中的卤原子: MQ a (2) 其中 M、Q 和 a 是在通式(1)所代表的化合物存在时定义的 1 其中 Z - 和 Rs 也已定义。
  • Courtot; Vignati, Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1927, vol. 184, p. 608
    作者:Courtot、Vignati
    DOI:——
    日期:——
  • Buu-Hoi; Lecocq, Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1948, vol. 226, p. 87
    作者:Buu-Hoi、Lecocq
    DOI:——
    日期:——
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