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30934-71-5

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30934-71-5 Usage

General Description

1-(1,2-dibromo-2-phenylethyl)-4-(trifluoromethyl)benzene is a chemical compound with the molecular formula C15H11Br2F3. It is a compound that contains both bromine and fluorine atoms, as well as a phenyl group. 1-(1,2-dibromo-2-phenylethyl)-4-(trifluoromethyl)benzene is often used as a reagent in chemical reactions, particularly in organic synthesis. It is known for its strong electrophilic and nucleophilic properties, which make it useful in a variety of chemical transformations. Additionally, this compound has potential applications in the pharmaceutical and agrochemical industries due to its unique structure and reactivity. Overall, 1-(1,2-dibromo-2-phenylethyl)-4-(trifluoromethyl)benzene is a versatile and important chemical compound with various industrial and research applications.

Check Digit Verification of cas no

The CAS Registry Mumber 30934-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,9,3 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30934-71:
(7*3)+(6*0)+(5*9)+(4*3)+(3*4)+(2*7)+(1*1)=105
105 % 10 = 5
So 30934-71-5 is a valid CAS Registry Number.

30934-71-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1,2-dibromo-2-phenylethyl)-4-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names -

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

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More Details:30934-71-5 SDS

30934-71-5Relevant articles and documents

Preassociation, free-ion, and ion-pair pathways in the electrophilic bromination of substituted cis- and trans-stilbenes in protic solvents

Ruasse, Marie-Fran?oise,Lo Moro, Giacomo,Galland, Bernard,Bianchini, Roberto,Chiappe, Cinzia,Bellucci, Giuseppe

, p. 12492 - 12502 (2007/10/03)

Rates and products of electrophilic bromination of ring-substituted cis- and trans-stilbenes have been investigated in acetic acid, trifluoroethanol, ethanol, methanol, and water-methanol mixtures. The mY(Br) relationships (linear for nucleophilic solvent

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