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126828-29-3

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126828-29-3 Usage

General Description

6-BROMO-1,1,2-TRIFLUOROHEX-1-ENE is a chemical compound with the molecular formula C6H8BrF3. It is a colorless liquid that is highly flammable and reactive. 6-BROMO-1,1,2-TRIFLUOROHEX-1-ENE is primarily used in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also used as a building block in the synthesis of more complex organic compounds. 6-BROMO-1,1,2-TRIFLUOROHEX-1-ENE is considered to be a hazardous material and should be handled with caution due to its toxicity and flammability.

Check Digit Verification of cas no

The CAS Registry Mumber 126828-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,2 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 126828-29:
(8*1)+(7*2)+(6*6)+(5*8)+(4*2)+(3*8)+(2*2)+(1*9)=143
143 % 10 = 3
So 126828-29-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H8BrF3/c7-4-2-1-3-5(8)6(9)10/h1-4H2

126828-29-3SDS

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 6-Bromo-1,1,2-trifluorohexene

1.2 Other means of identification

Product number -
Other names 6-BROMO-1,1,2-TRIFLUOROHEX-1-ENE

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:126828-29-3 SDS

126828-29-3Relevant articles and documents

Cyclization reactivities of fluorinated hex-5-enyl radicals

Dolbier Jr., William R.,Rong, Xiao X.,Bartberger, Michael D.,Koroniak, Henryk,Smart, Bruce E.,Yang, Zhen-Yu

, p. 219 - 231 (2007/10/03)

A kinetic study of the effect of fluorine substitution on the rates and regiochemistry of hex-5-enyl radical cyclization is reported. One or more fluorines on or proximate to the double bond of the radical have relatively little electronic effect on eithe

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