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702641-06-3

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702641-06-3 Usage

General Description

2-Iodo-5-(trifluoromethyl)benzyl bromide is a chemical compound with the molecular formula C8H6BrF3I. It is a benzyl bromide derivative that contains a trifluoromethyl group and an iodine atom attached to the benzene ring. 2-Iodo-5-(trifluoromethyl)benzyl bromide is commonly used in organic synthesis as a reagent for introducing the benzyl bromide group into other molecules. It is also known for its use in the pharmaceutical industry for the synthesis of various biologically active compounds. 2-Iodo-5-(trifluoromethyl)benzyl bromide is a highly reactive and versatile compound that has applications in research and development of new compounds. It should be handled with care and proper safety precautions as it is toxic and may be harmful if inhaled or ingested.

Check Digit Verification of cas no

The CAS Registry Mumber 702641-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,2,6,4 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 702641-06:
(8*7)+(7*0)+(6*2)+(5*6)+(4*4)+(3*1)+(2*0)+(1*6)=123
123 % 10 = 3
So 702641-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H5BrF3I/c9-4-5-3-6(8(10,11)12)1-2-7(5)13/h1-3H,4H2

702641-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Iodo-5-(Trifluoromethyl)Benzyl Bromide

1.2 Other means of identification

Product number -
Other names 2-(bromomethyl)-1-iodo-4-(trifluoromethyl)benzene

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:702641-06-3 SDS

702641-06-3Relevant articles and documents

Pd(II)-Catalyzed Synthesis of Benzocyclobutenes by β-Methylene-Selective C(sp3)-H Arylation with a Transient Directing Group

Chen, Xiangyang,Hoskin, John F.,Houk, K. N.,Provencher, Philip A.,Sorensen, Erik J.,Wong, Jonathan J.,Yu, Jin-Quan

supporting information, p. 20035 - 20041 (2021/12/09)

Methylene-selective C-H functionalization is a significant hurdle that remains to be addressed in the field of Pd(II) catalysis. We report a Pd(II)-catalyzed synthesis of benzocyclobutenes by methylene-selective C(sp3)-H arylation of ketones. The reaction utilizes glycine as a transient directing group and a 2-pyridone ligand, which may govern the methylene selectivity by making intimate molecular associations with the substrate during concerted metalation-deprotonation. This reaction is shown to be highly selective for intramolecular methylene C(sp3)-H arylation, thus enabling sequential C(sp3)-H functionalization.

Biphenyl-substituted oxazolidinones as cholesteryl ester transfer protein inhibitors: Modifications of the oxazolidinone ring leading to the discovery of anacetrapib

Smith, Cameron J.,Ali, Amjad,Hammond, Milton L.,Li, Hong,Lu, Zhijian,Napolitano, Joann,Taylor, Gayle E.,Thompson, Christopher F.,Anderson, Matt S.,Chen, Ying,Eveland, Suzanne S.,Guo, Qiu,Hyland, Sheryl A.,Milot, Denise P.,Sparrow, Carl P.,Wright, Samuel D.,Cumiskey, Anne-Marie,Latham, Melanie,Peterson, Laurence B.,Rosa, Ray,Pivnichny, James V.,Tong, Xinchun,Xu, Suoyu S.,Sinclair, Peter J.

experimental part, p. 4880 - 4895 (2011/09/20)

The development of the structure-activity studies leading to the discovery of anacetrapib is described. These studies focused on varying the substitution of the oxazolidinone ring of the 5-aryloxazolidinone system. Specifically, it was found that substitution of the 4-position with a methyl group with the cis-stereochemistry relative to the 5-aryl group afforded compounds with increased cholesteryl ester transfer protein (CETP) inhibition potency and a robust in vivo effect on increasing HDL-C levels in transgenic mice expressing cynomolgus monkey CETP.

NOVEL HETEROCYCLIDENE ACETAMIDE DERIVATIVE

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Page/Page column 107, (2010/11/30)

A compound represented by formula (I'): (wherein m, n, and p each represent 0 to 2; q represents 0 or 1; R1 represents halogen, a hydrocarbon group, a heterocyclic group, an alkoxy group, an alkoxycarbonyl group, a sulfamoyl group, a CN group,

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