Skip to Content
Merck
All Photos(3)

Key Documents

191167

Sigma-Aldrich

3-Nitrobenzyl chloride

97%

Synonym(s):

α-Chloro-3-nitrotoluene

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
O2NC6H4CH2Cl
CAS Number:
Molecular Weight:
171.58
Beilstein:
742794
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

solid

bp

85-87 °C/5 mmHg (lit.)

mp

43-47 °C (lit.)

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

Signal Word

Danger

Hazard Statements

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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service