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1,5-二溴-3-甲基戊烷 | 4457-72-1

中文名称
1,5-二溴-3-甲基戊烷
中文别名
3-甲基-1,5-二溴戊烷
英文名称
3-methyl-1,5-dibromopentane
英文别名
1,5-dibromo-3-methyl-pentane;1,5-Dibromo-3-methylpentane
1,5-二溴-3-甲基戊烷化学式
CAS
4457-72-1
化学式
C6H12Br2
mdl
——
分子量
243.969
InChiKey
YDPZWUMQKMLLHC-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

物化性质

  • 沸点:
    233℃
  • 密度:
    1.6
  • 闪点:
    101°(214°F)
  • 稳定性/保质期:
    在常温常压下保持稳定。

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    8
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 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
  • 安全说明:
    S24/25
  • 危险类别码:
    R36/37/38
  • 海关编码:
    2903399090
  • 危险性防范说明:
    P261,P264,P271,P280,P302+P352,P304+P340,P305+P351+P338,P312,P332+P313,P337+P313,P362,P403+P233,P405,P501
  • 危险性描述:
    H315,H319,H335
  • 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:ca7f982f88d95981e7070b5909a03404
查看
Name: 1 5-Dibromo-3-Methylpentane 98% Material Safety Data Sheet
Synonym: None known
CAS: 4457-72-1
Section 1 - Chemical Product MSDS Name:1 5-Dibromo-3-Methylpentane 98% Material Safety Data Sheet
Synonym:None known

Section 2 - COMPOSITION, INFORMATION ON INGREDIENTS
CAS# Chemical Name content EINECS#
4457-72-1 1,5-Dibromo-3-Methylpentane, 98% 98 unlisted
Hazard Symbols: None Listed.
Risk Phrases: None Listed.

Section 3 - HAZARDS IDENTIFICATION
EMERGENCY OVERVIEW
The toxicological properties of this material have not been fully investigated.
Potential Health Effects
Eye:
May cause eye irritation.
Skin:
May cause skin irritation.
Ingestion:
May cause irritation of the digestive tract. The toxicological properties of this substance have not been fully investigated.
Inhalation:
May cause respiratory tract irritation. The toxicological properties of this substance have not been fully investigated.
Chronic:
No information found.

Section 4 - FIRST AID MEASURES
Eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid.
Skin:
Get medical aid. Flush skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes. Wash clothing before reuse.
Ingestion:
Never give anything by mouth to an unconscious person. Get medical aid. Do NOT induce vomiting. If conscious and alert, rinse mouth and drink 2-4 cupfuls of milk or water.
Inhalation:
Remove from exposure and move to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical aid.
Notes to Physician:

Section 5 - FIRE FIGHTING MEASURES
General Information:
As in any fire, wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear. During a fire, irritating and highly toxic gases may be generated by thermal decomposition or combustion. Use water spray to keep fire-exposed containers cool. Vapors may be heavier than air. They can spread along the ground and collect in low or confined areas. Containers may explode when heated.
Extinguishing Media:
Use agent most appropriate to extinguish fire. Cool containers with flooding quantities of water until well after fire is out. Use water spray, dry chemical, carbon dioxide, or appropriate foam.

Section 6 - ACCIDENTAL RELEASE MEASURES
General Information: Use proper personal protective equipment as indicated in Section 8.
Spills/Leaks:
Vacuum or sweep up material and place into a suitable disposal container. Clean up spills immediately, observing precautions in the Protective Equipment section. Avoid generating dusty conditions.
Provide ventilation.

Section 7 - HANDLING and STORAGE
Handling:
Wash thoroughly after handling. Remove contaminated clothing and wash before reuse. Use with adequate ventilation. Minimize dust generation and accumulation. Avoid contact with eyes, skin, and clothing. Keep container tightly closed. Avoid ingestion and inhalation.
Storage:
Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

Section 8 - EXPOSURE CONTROLS, PERSONAL PROTECTION
Engineering Controls:
Facilities storing or utilizing this material should be equipped with an eyewash facility and a safety shower. Use adequate ventilation to keep airborne concentrations low.
Exposure Limits CAS# 4457-72-1: Personal Protective Equipment Eyes: Wear appropriate protective eyeglasses or chemical safety goggles as described by OSHA's eye and face protection regulations in 29 CFR 1910.133 or European Standard EN166.
Skin:
Wear appropriate protective gloves to prevent skin exposure.
Clothing:
Wear appropriate protective clothing to prevent skin exposure.
Respirators:
A respiratory protection program that meets OSHA's 29 CFR 1910.134 and ANSI Z88.2 requirements or European Standard EN 149 must be followed whenever workplace conditions warrant respirator use.

Section 9 - PHYSICAL AND CHEMICAL PROPERTIES

Physical State: Liquid
Color: clear, colorless
Odor: bromine-like
pH: Not available.
Vapor Pressure: Not available.
Viscosity: Not available.
Boiling Point: Not available.
Freezing/Melting Point: Not available.
Autoignition Temperature: Not available.
Flash Point: Not available.
Explosion Limits, lower: Not available.
Explosion Limits, upper: Not available.
Decomposition Temperature:
Solubility in water:
Specific Gravity/Density: 1.6086g/cm3
Molecular Formula: C6H12Br2
Molecular Weight: 243.97

Section 10 - STABILITY AND REACTIVITY
Chemical Stability:
Stable under normal temperatures and pressures.
Conditions to Avoid:
Incompatible materials, excess heat, strong oxidants.
Incompatibilities with Other Materials:
Oxidizing agents.
Hazardous Decomposition Products:
Carbon monoxide, irritating and toxic fumes and gases, carbon dioxide, hydrogen bromide.
Hazardous Polymerization: Has not been reported

Section 11 - TOXICOLOGICAL INFORMATION
RTECS#:
CAS# 4457-72-1 unlisted.
LD50/LC50:
Not available.
Carcinogenicity:
1,5-Dibromo-3-Methylpentane, 98% - Not listed by ACGIH, IARC, or NTP.

Section 12 - ECOLOGICAL INFORMATION


Section 13 - DISPOSAL CONSIDERATIONS
Dispose of in a manner consistent with federal, state, and local regulations.

Section 14 - TRANSPORT INFORMATION

IATA
Not regulated as a hazardous material.
IMO
Not regulated as a hazardous material.
RID/ADR
Not regulated as a hazardous material.

Section 15 - REGULATORY INFORMATION

European/International Regulations
European Labeling in Accordance with EC Directives
Hazard Symbols: Not available.
Risk Phrases:
Safety Phrases:
S 24/25 Avoid contact with skin and eyes.
S 28A After contact with skin, wash immediately with
plenty of water.
S 37 Wear suitable gloves.
S 45 In case of accident or if you feel unwell, seek
medical advice immediately (show the label where
possible).
WGK (Water Danger/Protection)
CAS# 4457-72-1: No information available.
Canada
None of the chemicals in this product are listed on the DSL/NDSL list.
CAS# 4457-72-1 is not listed on Canada's Ingredient Disclosure List.
US FEDERAL
TSCA
CAS# 4457-72-1 is not listed on the TSCA inventory.
It is for research and development use only.


SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

  • 作为反应物:
    描述:
    1,5-二溴-3-甲基戊烷magnesium 、 sodium iodide 作用下, 以 1,4-二氧六环乙醚丙酮 为溶剂, 反应 6.5h, 生成 5-methyl-8-hexadecyn-1-ol
    参考文献:
    名称:
    摘要:
    Difficulties in isolating and purifying antibiotic fatty acids from culture filtrates of Pseudozyma flocculosa, a biocontrol agent against powdery mildew, have been limiting factors in studying the properties and understanding the mode of action of the biocontrol agent. We report a new protocol for synthesizing (Z)-9-heptadecenoic and for the first time synthesis of (Z)-6-methyl-9-heptadecenoic acids, two antibiotic fatty acids produced by P. flocculosa. This allowed reproducible and quantifiable means of assaying biological activity of the molecules. In these bioassays, both molecules exhibited antifungal activity corresponding to their expected potency. These new developments should facilitate further studies aimed at deciphering the ecological properties of P. flocculosa.
    DOI:
    10.1023/a:1005464326573
  • 作为产物:
    描述:
    四氢-4-甲基-2H-吡喃硫酸氢溴酸 作用下, 反应 3.0h, 以79%的产率得到1,5-二溴-3-甲基戊烷
    参考文献:
    名称:
    昆虫的信息素及其类似物。二十九。来自 4-甲基四氢吡喃 4 的甲基支化信息素: (?)-15,19,23-trimethylheptacontane 的合成?Glossina morsitans morsitans 的信息素
    摘要:
    外消旋 15,19,23-trimethylheptacontane(舌蝇Glossina morsitans morsitans 的性信息素)是由 1,5-dibromo-3-methylpentane(4-甲基四氢吡喃酸水解的产物)合成的。
    DOI:
    10.1007/bf00630327
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文献信息

  • Asymmetric Cycloetherification of in Situ Generated Cyanohydrins through the Concomitant Construction of Three Chiral Carbon Centers
    作者:Yosuke Kurimoto、Teruhisa Nasu、Yuki Fujii、Keisuke Asano、Seijiro Matsubara
    DOI:10.1021/acs.orglett.9b00462
    日期:2019.4.5
    cyanohydrins through the concomitant construction of three chiral carbon centers is reported. This protocol facilitates the concise synthesis of optically active tetrahydropyran derivatives, which are ubiquitous scaffolds found in various bioactive compounds, through the simultaneous construction of multiple bonds and stereogenic centers, including tetrasubstituted chiral carbons. The resulting products
    据报道,通过同时构筑三个手性碳中心,就可以对原位生成的氰醇进行有机催化的对映体和非对映体选择性环醚化。该协议通过同时构建多个键和立体中心(包括四取代的手性碳原子),促进了光学活性四氢吡喃衍生物的简明合成,该衍生物是在各种生物活性化合物中普遍存在的支架。所得产物还包含多个合成上重要的官能团,这些官能团扩展了它们作为手性结构单元的可能用途。
  • Enantio- and Diastereoselective Construction of Contiguous Tetrasubstituted Chiral Carbons in Organocatalytic Oxadecalin Synthesis
    作者:Yuuki Wada、Ryuichi Murata、Yuki Fujii、Keisuke Asano、Seijiro Matsubara
    DOI:10.1021/acs.orglett.0c01501
    日期:2020.6.19
    The organocatalytic enantio- and diastereoselective cycloetherification of 1,3-cyclohexanedione-bearing enones involving the in situ generation of chiral cyanohydrins was developed. This transformation offers the first catalytic asymmetric approach to oxadecalin derivatives containing contiguous tetrasubstituted chiral carbons at the bridge heads of the fused ring systems. Depending on substituents
    已开发了涉及1,3-环己二酮的烯酮的有机催化对映和非对映选择性环醚化反应,涉及手性氰醇的原位生成。这种转变为在稠环系统桥头处含有连续四取代手性碳的奥沙德林衍生物提供了第一种催化不对称方法。根据取代基的不同,合成的顺式和反式十氢化萘型支架均具有良好的立体选择性,以及在反式-oxadecalin衍生物的手性季碳部分上积累的一系列官能团。
  • [DE] 3-(4-PIPERIDIN-1YLMETHYL-PHENYL) -PROPIONSÄURE-PHRNYLAMID-DERIVATE UND VERWANDTE VERBINDUNGEN ALS MCH (MELANINE CONCENTRATING HORMONE) ANTAGONISTEN ZUR BEHANDLUNG VON ESSSTÖRUNGEN<br/>[EN] 3-(4-PIPERIDINE-1YLMETHYL-PHENYL)-PROPION ACID-PHENYLAMIDE-DERIVATIVES AND RELATED COMPOUNDS USED IN THE FORM OF MCH ANTAGONISTS (MELANINE CONCENTRATING HORMONE) FOR TREATING EATING DISORDERS<br/>[FR] DERIVES D'ACIDE 3-(4-PIPERIDINE-1YLMETHYL-PHENYL) PROPIONIQUE-PHENYLAMIDE ET COMPOSES APPARENTES, UTILISES COMME ANTAGONISTES MCH (HORMONE DE CONCENTRATION EN MELANINE) POUR LE TRAITEMENT DE TROUBLES DUS A L'ALIMENTATION
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2005063239A1
    公开(公告)日:2005-07-14
    Die vorliegende Erfindung betrifft Amid-Verbindungen der allgemeinen Formel (I), in der die Gruppen und Reste A, B, b, W, X, Y, Z, R1, R2 und R3 die in Anspruch 1 angegebenen Bedeutungen aufweisen. Ferner betrifft die Erfindung Arzneimittel enthaltend mindestens ein erfindungsgemäßes Amid. Auf Grund der MCH-Rezeptor antagonistischen Aktivität eignen sich die erfindungsgemäßen Arzneimittel zur Behandlung von metabolischen Störungen und/oder Essstörungen, insbesondere von Adipositas, Bulimie, Anorexie, Hyperphagia und Diabetes.
    该发明涉及通式(I)的酰胺化合物,其中基团和残基A、B、b、W、X、Y、Z、R1、R2和R3具有权利要求1中所述的含义。此外,该发明涉及含有至少一种根据本发明的酰胺的药物。由于MCH受体拮抗活性,根据本发明的药物适用于治疗代谢紊乱和/或进食障碍,特别是肥胖症、暴食症、厌食症、过度进食和糖尿病。
  • 作为丙型肝炎抑制剂的螺环化合物及其在药 物中的应用
    申请人:广东东阳光药业有限公司
    公开号:CN103880823B
    公开(公告)日:2017-12-05
    本发明提供了作为丙型肝炎抑制剂的螺环化合物及其在药物中的用途。所述一种化合物为式(I)所示的化合物或式(I)所示化合物的立体异构体、几何异构体、互变异构体、氮氧化物、水合物、溶剂化物、代谢产物、药学上可接受的盐或前药。此外,本发明还提供了包含所述化合物的药物组合物,所述化合物和所述药物组合物用于抑制HCV复制和抑制HCV病毒蛋白功能的至少之一的用途,以及所述化合物和所述药物组合物用于预防、处理、治疗或减轻患者的HCV感染或丙型肝炎疾病的用途。
  • PYRIDONE COMPOUNDS AND AGRICULTURAL AND HORTICULTURAL FUNGICIDES CONTAINING THE SAME AS ACTIVE INGREDIENTS
    申请人:MITSUI CHEMICALS AGRO, INC.
    公开号:US20200172486A1
    公开(公告)日:2020-06-04
    Provided are a pyridone compound represented by Formula (1): wherein R1 represents a C1-C6 alkyl group which may be substituted, etc., R2 represents a halogen atom, a cyano group, etc., R3 and R4 are independent to each other, and each represents a hydrogen atom, a C1-C6 alkyl group which may be substituted, etc., or in combination with the nitrogen atom to which they are bonded form a pyrrolidinyl group, a piperidinyl group, etc., which may be substituted, Y represents a phenyl group which may be substituted, etc., X represents an oxygen atom or a sulfur atom, and an agricultural and horticultural fungicide containing the same as an active ingredient.
    提供的是由化学式(1)表示的吡啶酮化合物: 其中 R1代表一个可能被取代的C1-C6烷基,等等, R2代表一个卤素原子,一个氰基,等等, R3和R4彼此独立,每个代表一个氢原子,一个可能被取代的C1-C6烷基,等等,或者与它们结合的氮原子形成一个可能被取代的吡咯啉基团,一个哌啶基团,等等, Y代表一个可能被取代的苯基,等等, X代表一个氧原子或硫原子, 以及含有该化合物作为活性成分的农业和园艺用杀菌剂。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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mass
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ir
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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