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C27115

Sigma-Aldrich

4-Chlorobenzyl alcohol

99%

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Synonym(s):
1-Chloro-4-(hydroxymethyl)benzene, 4-Chlorobenzenemethanol, 4-Chlorophenylmethanol, p-Chlorobenzyl alcohol, p-Chlorotoluol
Linear Formula:
ClC6H4CH2OH
CAS Number:
Molecular Weight:
142.58
Beilstein/REAXYS Number:
636502
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

form

crystals

bp

234 °C (lit.)

mp

68-71 °C (lit.)

SMILES string

OCc1ccc(Cl)cc1

InChI

1S/C7H7ClO/c8-7-3-1-6(5-9)2-4-7/h1-4,9H,5H2

InChI key

PTHGDVCPCZKZKR-UHFFFAOYSA-N

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1 of 4

This Item
183431183423100293
4-Chlorobenzyl alcohol 99%

C27115

4-Chlorobenzyl alcohol

4-Bromophenethyl alcohol 99%

183431

4-Bromophenethyl alcohol

4-Chlorophenethyl alcohol 99%

183423

4-Chlorophenethyl alcohol

2,6-Dichlorobenzyl alcohol 99%

100293

2,6-Dichlorobenzyl alcohol

mp

68-71 °C (lit.)

mp

-

mp

-

mp

96-98 °C (lit.)

bp

234 °C (lit.)

bp

138 °C/9 mmHg (lit.)

bp

110 °C/0.5 mmHg (lit.)

bp

-

form

crystals

form

liquid

form

-

form

solid

Application

Reagent for carboxyl group protection.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Customers Also Viewed

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1 of 1

Mario Silva et al.
Journal of chromatography. A, 1629, 461508-461508 (2020-08-29)
In the present document, we report the development of an analytical method consisting of a sequential direct-immersion/headspace solid-phase microextraction (DI-HS-SPME) followed by gas-phase chromatography and tandem mass spectrometry (GC-MS/MS) for simultaneous analysis of 4-chlorobenzyl alcohol, 2,6-dichlorobenzyl alcohol, 4-methoxybenzyl alcohol, 3,4-dimethoxybenzyl
Kenji Matsuno et al.
Bioorganic & medicinal chemistry letters, 20(17), 5126-5129 (2010-08-07)
S-benzylisothiourea 3a was discovered by its ability to inhibit indoleamine-2,3-dioxygenase (IDO) in our screening program. Subsequent optimization of the initial hit 3a lead to the identification of sub-muM inhibitors 3r and 10h, both of which suppressed kynurenine production in A431

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