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C27115

Sigma-Aldrich

4-Chlorobenzyl alcohol

99%

Synonym(s):

1-Chloro-4-(hydroxymethyl)benzene, 4-Chlorobenzenemethanol, 4-Chlorophenylmethanol, p-Chlorobenzyl alcohol, p-Chlorotoluol

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About This Item

Linear Formula:
ClC6H4CH2OH
CAS Number:
873-76-7
Molecular Weight:
142.58
Beilstein:
636502
EC Number:
212-852-2
MDL number:
MFCD00004652
UNSPSC Code:
12352100
PubChem Substance ID:
24892520
NACRES:
NA.22

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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Application

Reagent for carboxyl group protection.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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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