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95896-86-9

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95896-86-9 Usage

Physical state

Colorless liquid

Uses

Intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds

Chemical reactivity

Can undergo addition, substitution, and elimination reactions

Versatility

Acts as a versatile building block in organic synthesis

Safety

Flammable and potentially hazardous substance, requires careful handling

Importance

Plays a crucial role in the pharmaceutical and chemical industries due to its reactivity and versatility in organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 95896-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,8,9 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 95896-86:
(7*9)+(6*5)+(5*8)+(4*9)+(3*6)+(2*8)+(1*6)=209
209 % 10 = 9
So 95896-86-9 is a valid CAS Registry Number.

95896-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-Cyclohexadiene, 1-bromo-

1.2 Other means of identification

Product number -
Other names 1-Bromo-1,4-cyclohexadiene

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:95896-86-9 SDS

95896-86-9Relevant articles and documents

Cycloallenes, 13. - Cyclohexa-1,2,4-triene from 1-bromocyclohexa-1,4- diene

Christl, Manfred,Groetsch, Stefan

, p. 1871 - 1874 (2007/10/03)

1-Bromocyclohexa-1,4-diene (3) was prepared from trans-4,5- dibromocyclohexene by elimination of hydrogen bromide. Treatment of a solution of 3 in furan or 2,5-dimethylfuran with KOtBu afforded the tetrahydroepoxynaphthalenes 4 and 5, respectively. The st

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