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Safety Information

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

C27115-25G:
C27115-VAR:
C27115-100G:
C27115-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
STBG9541
STBB6975V
STBB6975
07918BJ
S46707

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4-(Chloromethyl)benzyl alcohol 99%

Sigma-Aldrich

526126

4-(Chloromethyl)benzyl alcohol

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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