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1-BROMO-2-(BROMODIFLUOROMETHYL)CYCLOHEXANE, with the molecular formula C7H8Br2F2, is a colorless liquid that belongs to the class of halogenated compounds. It is characterized by the presence of bromine and fluorine atoms, which contribute to its unique chemical properties. 1-BROMO-2-(BROMODIFLUOROMETHYL)CYCLOHEXANE is primarily utilized as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and also serves as a solvent and in the production of other organic compounds.

14737-09-8

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14737-09-8 Usage

Uses

Used in Pharmaceutical Industry:
1-BROMO-2-(BROMODIFLUOROMETHYL)CYCLOHEXANE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 1-BROMO-2-(BROMODIFLUOROMETHYL)CYCLOHEXANE is employed as an intermediate in the production of agrochemicals. Its properties enable the creation of effective compounds for pest control and crop protection.
Used as a Solvent:
1-BROMO-2-(BROMODIFLUOROMETHYL)CYCLOHEXANE is utilized as a solvent in various chemical processes. Its ability to dissolve a wide range of substances makes it a valuable component in the synthesis of other organic compounds.
Used in Synthesis of Other Organic Compounds:
1-BROMO-2-(BROMODIFLUOROMETHYL)CYCLOHEXANE is also used in the synthesis of other organic compounds, where its unique structure and properties contribute to the formation of new and useful chemical entities.
Safety Precautions:

Check Digit Verification of cas no

The CAS Registry Mumber 14737-09-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,3 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14737-09:
(7*1)+(6*4)+(5*7)+(4*3)+(3*7)+(2*0)+(1*9)=108
108 % 10 = 8
So 14737-09-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H7ClF3NO/c15-10-3-1-8(2-4-10)9-5-12(14(16,17)18)11(7-19)13(20)6-9/h1-6,20H

14737-09-8SDS

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-Bromo-2-(bromodifluoromethyl)-cyclohexane

1.2 Other means of identification

Product number -
Other names 1-BROMO-2-(BROMODIFLUOROMETHYL)CYCLOHEXANE

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:14737-09-8 SDS

14737-09-8Relevant academic research and scientific papers

Mechanistic Studies on Zinc-Induced Addition of CF2Br2 to Olefins. A Novel Radical Reductive Cyclopropanation on the Zinc Surface

Wu, Shi-Hui,Liu, Wei-Zhong,Jiang, Xi-Kui

, p. 854 - 857 (1994)

The addition reaction of dibromodifluoromethane (1) to olefins induced by zinc in ethereal solvent differs surprisingly from addition reactions hitherto reported.Both cyclopropane derivatives and 1:1 addition products were obtained from this reaction.A free-radical chain addition reaction induced by single electron transfer (SET) is proposed.This reaction is inhibited by hydroquinone and completely quenched by p-dinitrobenzene.The nature of the 1:1 adducts formed revealed the character of a typical radical reaction.The nature of the cyclopropane derivatives formed was also much different from the usual cyclopropane adduct derived from carbene addition.When diallyl ether (15) and norbornadiene (16) were used as substrates, only rearranged 1:1 addition products could be obtained, and no cyclopropane product could be detected.The results of addition reactions with 4-octenes (27) showed also that the cyclopropanation reaction was not stereospecific.On the basis of the above-mentioned results, a novel reductive debromocyclopropanation reaction of the γ-bromopropyl radical intermediate proceeding on the zinc metal surface is suggested.

Synthesis of bromodifluoromethyl-substituted alkenes. Potassium fluoride supported on alumina as a dehydrobrominating agent

Hu, Chang-Ming,Chen, Jian

, p. 25 - 26 (2007/10/02)

Potassium fluoride supported on alumina is an efficient dehydrobrominating agent. 1,3-Dibromo-1,1-difluoroalkanes - adducts of dibromodifluoromethane and alkenes - give bromodifluoromethyl-substituted alkenes 2 on dehydrobromination with this agent in goo

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