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Merck
CN

363901

2-Chloro-2-propen-1-ol

technical grade, 90%

Synonym(s):

2-Chloroallyl alcohol

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About This Item

Linear Formula:
H2C=C(Cl)CH2OH
CAS Number:
Molecular Weight:
92.52
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
90%
Form:
liquid
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grade

technical grade

Quality Level

assay

90%

form

liquid

refractive index

n20/D 1.459 (lit.)

bp

133-134 °C (lit.)

density

1.162 g/mL at 25 °C (lit.)

functional group

chloro, hydroxyl

SMILES string

OCC(Cl)=C

InChI

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

InChI key

OSCXYTRISGREIM-UHFFFAOYSA-N

General description

2-Chloro-2-propen-1-ol is reported to undergo photodissociation at 193nm to generate CH2CCH2OH radical intermediate. 2-Chloro-2-propen-1-ol is formed as major product during base mediated reaction of 1,2,3-trichloropropane. 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.

Application

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


pictograms

FlameExclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

129.2 °F - closed cup

flash_point_c

54 °C - closed cup

ppe

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

Regulatory Information

危险化学品

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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
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



Global Trade Item Number

SKUGTIN
363901-5G04061837073144
363901-25G04061837073137