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363901

Sigma-Aldrich

2-Chloro-2-propen-1-ol

technical grade, 90%

동의어(들):

2-Chloroallyl alcohol

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5 G
₩89,929
25 G
₩294,553

₩89,929

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모든 사진(1)

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5 G
₩89,929
25 G
₩294,553

About This Item

Linear Formula:
H2C=C(Cl)CH2OH
CAS Number:
5976-47-6
Molecular Weight:
92.52
MDL number:
MFCD00004701
UNSPSC 코드:
12352100
PubChem Substance ID:
24862371
NACRES:
NA.22

₩89,929

구입 가능 여부는 고객센터에 문의하십시오.
벌크 견적 요청

Grade

technical grade

Quality Level

100

분석

90%

양식

liquid

refractive index

n20/D 1.459 (lit.)

bp

133-134 °C (lit.)

density

1.162 g/mL at 25 °C (lit.)

작용기

chloro
hydroxyl

SMILES string

OCC(Cl)=C

InChI

1S/C3H5ClO/c1-3(4)2-5/h5H,1-2H2

InChI key

OSCXYTRISGREIM-UHFFFAOYSA-N

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관련 카테고리

일반 설명

2-Chloro-2-propen-1-ol is reported to undergo photodissociation at 193nm to generate CH2CCH2OH radical intermediate.[1] 2-Chloro-2-propen-1-ol is formed as major product during base mediated reaction of 1,2,3-trichloropropane.[2] 2-Chloro-2-propen-1-ol is reported to react with phosphorus trichloride to yield phosphorous esters, while with phosphory chloride it yields phosphoric ester.[3]

애플리케이션

2-Chloro-2-propen-1-ol (2-chloropropenol) may be employed as carbon supplement for the growth of Pseudomonas strains.[4] It may be used in the preparation of 2-(4-octylphenyl)prop-2-en-1-ol.[5]

픽토그램

FlameExclamation mark
GHS02,GHS07

신호어

Warning

유해 및 위험 성명서

H226,H302 + H312 + H332

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point (°F)

129.2 °F - closed cup

Flash Point (°C)

54 °C - closed cup

개인 보호 장비

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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시험 성적서(COA)

Lot/Batch Number
MKCT2418
MKCH9010
MKBS0376V
MKBP8748V
MKBD8116V

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문서 라이브러리 방문

Kinetic studies of the homogeneous abiotic reactions of several chlorinated aliphatic compounds in aqueous solution.
Pagan M, et al.
Applied Geochemistry, 13(6), 779-785 (1998)
J J van der Waarde et al.
Applied and environmental microbiology, 59(2), 528-535 (1993-02-01)
Three Pseudomonas strains capable of utilizing 2-chloroallylalcohol (2-chloropropenol) as the sole carbon source for growth were isolated from soil. The fastest growth was observed with strain JD2, with a generation time of 3.6 h. Degradation of 2-chloroallylalcohol was accompanied by
Derivatives of phosphorus acids and 2-chloro-2-propen-1-ol.
Arbuzov BA, et al.
Russian Chemical Bulletin, 16(6), 1233-1238 (1967)
Arjun S Raman et al.
The Journal of chemical physics, 127(15), 154316-154316 (2007-10-24)
These velocity map imaging experiments characterize the photolytic generation of one of the two radical intermediates formed when OH reacts via an addition mechanism with allene. The CH2CCH2OH radical intermediate is generated photolytically from the photodissociation of 2-chloro-2-propen-1-ol at 193
Ran Zhu et al.
Journal of medicinal chemistry, 50(25), 6428-6435 (2007-11-13)
Compound 1 (FTY720, Fingolimod) represents a new generation of immunosuppressant that modulates lymphocyte trafficking by interacting with the S1P(1) receptor. Compound 1 also provides a template molecule for studying the molecular biology of S1P receptors and related enzymes (kinases and
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