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140112

4-Nitrobenzyl chloride

99%

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Synonym(s):

α-Chloro-4-nitrotoluene

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25 g

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$76.70
100 g
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$247.00

About This Item

Linear Formula:
O2NC6H4CH2Cl
CAS Number:
Molecular Weight:
171.58
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-822-7
Beilstein/REAXYS Number:
387187
MDL number:
Assay:
99%
Form:
solid

$76.70


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Quality Segment

assay

99%

form

solid

mp

70-73 °C (lit.)

solubility

chloroform: soluble 50 mg/mL, clear to very slightly hazy, faintly yellow

functional group

chloro, nitro

SMILES string

[O-][N+](=O)c1ccc(CCl)cc1

InChI

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

InChI key

KGCNHWXDPDPSBV-UHFFFAOYSA-N

General description

4-Nitrobenzyl chloride acts as substrate for glutathione S-transferase(GST) in determination of GST in Chinese fetal liver. It undergoes reduction by NADPH to yield 4-nitrotoluene.

Application

4-Nitrobenzyl chloride was used to prepare unsymmetrically N,N′-bis(substituted) 4,13-diaza-18-crown-6-ether derivatives.

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This Item
73120114081188271
description

99%

description

derivatization grade (HPLC), LiChropur, ≥99.0% (GC)

description

97%

description

98%

assay

99%

assay

≥99.0% (GC)

assay

97%

assay

98%

solubility

chloroform: soluble 50 mg/mL, clear to very slightly hazy, faintly yellow

solubility

-

solubility

-

solubility

-

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

200

form

solid

form

crystals

form

solid

form

-

mp

70-73 °C (lit.)

mp

71-74 °C

mp

77-79 °C (lit.)

mp

90-92 °C (lit.)

functional group

chloro, nitro

functional group

-

functional group

phenyl, chloro

functional group

nitro, chloro, hydroxyl


pictograms

CorrosionExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges



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