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주요 문서

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A30702

Sigma-Aldrich

Allyl chloride

reagent grade, 98%

동의어(들):

3-Chloro-1-propene, Chlorallylene

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모든 사진(3)

About This Item

Linear Formula:
CH2=CHCH2Cl
CAS Number:
107-05-1
Molecular Weight:
76.52
Beilstein:
635704
EC Number:
203-457-6
MDL number:
MFCD00000984
UNSPSC 코드:
12352100
PubChem Substance ID:
57653821
NACRES:
NA.22

Grade

reagent grade

Quality Level

200

vapor density

2.6 (vs air)

vapor pressure

20.58 psi ( 55 °C)
5.71 psi ( 20 °C)

분석

98%

양식

liquid

expl. lim.

11.2 %

refractive index

n20/D 1.414 (lit.)

bp

44-46 °C (lit.)

mp

−130 °C (lit.)

density

0.939 g/mL at 25 °C (lit.)

저장 온도

2-8°C

SMILES string

ClCC=C

InChI

1S/C3H5Cl/c1-2-3-4/h2H,1,3H2

InChI key

OSDWBNJEKMUWAV-UHFFFAOYSA-N

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관련 카테고리

애플리케이션

Allyl chloride can be used as a reactant to prepare:
  • 1-Allyl-2-alkynylbenzene derivatives through allylalkynylation of in situ generated benzynes.
  • α,ω-Difunctional intermediates by reacting with fatty acid methyl esters using ruthenium catalysts.
  • Homoallylic alcohols through Sn/I2 catalyzed Barbier-type allylation reactions of carbonyl compounds.

기타 정보

The article number A30702-4X1L will be discontinued. Please order the single bottle A30702-1L which is physically identical with the same exact specifications.

신호어

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - Muta. 2 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3

표적 기관

Nervous system,Liver,Kidney, Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point (°F)

-25.6 °F

Flash Point (°C)

-32 °C

개인 보호 장비

Eyeshields, Faceshields, Gloves

가장 최신 버전 중 하나를 선택하세요:

시험 성적서(COA)

Lot/Batch Number
STBK6237
STBK3443
STBK2239
SHBN1816
WXBD2636V

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COA 검색

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문서 라이브러리 방문

이미 열람한 고객

Slide 1 of 2

1 of 2

Allyl alcohol ≥99%

Sigma-Aldrich

240532

Allyl alcohol

11-Chloro-1-undecene 97%

Sigma-Aldrich

593117

11-Chloro-1-undecene

Airong Xu et al.
Polymers, 11(5) (2019-05-15)
Cellulose is the most abundant natural biopolymer, with unique properties such as biodegradability, biocompability, nontoxicity, and so on. However, its extensive application has actually been hindered, because of its insolubility in water and most solvents. Herein, highly efficient cellulose solvents
Airong Xu et al.
Scientific reports, 9(1), 11518-11518 (2019-08-10)
The utilization of cellulose in industrial applicat is of great significance to sustainable development of human society and reducing dependence on dwindling fossil resources. Nevertheless, this utilization of cellulose has actually been limited due to its insolubilization. Here, novel solvents
Sn/I2 Mediated allylation of carbonyl compounds with allyl (crotyl) halide in water
Zhou Y, et al.
ARKIVOC (Gainesville, FL, United States), 11(1), 142-153 (2008)
Carbocycle synthesis through facile and efficient palladium-catalyzed allylative de-aromatization of naphthalene and phenanthrene allyl chlorides.
Shirong Lu et al.
Angewandte Chemie (International ed. in English), 47(23), 4366-4369 (2008-04-30)
Vikas Sikervar et al.
The Journal of organic chemistry, 77(11), 5132-5138 (2012-04-27)
A coupling strategy for the synthesis of 2,4-dimethyl-1α,25(OH)(2)D(3) is achieved which involves methylation of a pro-A ring vinyl sulfone and in situ traping of the allyl sulfonyl anion with a CD ring allyl chloride. TBAF-promoted 1,2-eliminative desulfonylation and concomitant silyl
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