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7559-38-8

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7559-38-8 Usage

Appearance

Yellow crystalline powder

Usage

Building block in organic synthesis

Applications

a. Production of pharmaceuticals
b. Production of agrochemicals
c. Production of dyes
d. Manufacturing of explosives
e. Manufacturing of rubber chemicals
f. Manufacturing of polymer additives

Reactivity

High reactivity

Safety

Handled with caution due to toxic and potentially hazardous nature

Check Digit Verification of cas no

The CAS Registry Mumber 7559-38-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,5 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7559-38:
(6*7)+(5*5)+(4*5)+(3*9)+(2*3)+(1*8)=128
128 % 10 = 8
So 7559-38-8 is a valid CAS Registry Number.

7559-38-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(E)-2-bromo-2-nitroethenyl]-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names 1-(2-bromo-2-nitrovinyl)-4-nitrobenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7559-38-8 SDS

7559-38-8Relevant articles and documents

Synthesis and [3+2] cycloadditions of 3-bromo-5,6-dihydro-4 H -1,2-oxazine N -oxides

Romashov, Leonid V.,Khomutova, Yulya A.,Danilenko, Vitaliy M.,Ioffe, Sema L.,Lesiv, Alexey V.

experimental part, p. 407 - 414 (2010/05/18)

A number of 3-bromo-5,6-dihydro-4H-1,2-oxazine N-oxides have been synthesized and subjected to [3+2] cycloaddition with alkenes affording various types of products: 3-vinyloxazolines, isoxazoline N-oxides, and 3-functionalized 1,2-oxazine N-oxides. Georg Thieme Verlag Stuttgart - New York.

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