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191167

Sigma-Aldrich

3-Nitrobenzyl chloride

97%

Synonym(s):

α-Chloro-3-nitrotoluene

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About This Item

Linear Formula:
O2NC6H4CH2Cl
CAS Number:
619-23-8
Molecular Weight:
171.58
Beilstein:
742794
EC Number:
210-586-1
MDL number:
MFCD00007272
UNSPSC Code:
12352100
PubChem Substance ID:
24851471
NACRES:
NA.22

Assay

97%

form

solid

bp

85-87 °C/5 mmHg (lit.)

mp

43-47 °C (lit.)

functional group

chloro

SMILES string

[O-][N+](=O)c1cccc(CCl)c1

InChI

1S/C7H6ClNO2/c8-5-6-2-1-3-7(4-6)9(10)11/h1-4H,5H2

InChI key

APGGSERFJKEWFG-UHFFFAOYSA-N

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General description

Influence of solvent on reduction mechanism of 3-nitrobenzyl chloride was investigated by cyclic voltammetry and controlled potential bulk electrolysis.

Application

3-Nitrobenzyl chloride was used in the synthesis of 8-chloropurine.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

230.0 °F - closed cup

Flash Point(C)

110 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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J L Kelley et al.
Journal of medicinal chemistry, 33(1), 196-202 (1990-01-01)
A series of 8-substituted analogues of 9-(3-aminobenzyl)-6-(dimethylamino)-9H-purine (8) were synthesized and tested for their ability to bind to the benzodiazepine receptor (BZR) in rat brain tissue. The most active compound was the 8-bromo-9-(3-formamidobenzyl) analogue 16 (IC50 = 0.011 microM), which
Solvent effects on the reduction mechanism of 3-chloroanthracene, 3-nitrobenzyl chloride and 3-chloroacetophenone.
Jensen H and Daasbjerg K
Acta Chirurgica Scandinavica. Supplementum, 58, 1151-1164 (1998)

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