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2,3,5,6-Tetrafluoro-4-(trifluoromethyl)benzyl bromide, also known as TTBB, is a chemical compound that can be used as an alternative to pentafluorobenzyl bromide (PFBB) in electrophoric derivatization reactions. It is characterized by its tetrafluoro and trifluoromethyl groups attached to a benzyl bromide structure, which allows for effective derivatization of various compounds.

76437-40-6

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76437-40-6 Usage

Uses

Used in Analytical Chemistry:
TTBB is used as a derivatization reagent for the characterization and quantitation of DNA and hemoglobin adducts. Its unique structure allows for effective labeling and detection of these biologically significant molecules, enhancing the sensitivity and accuracy of analytical techniques.
Used in Gas Chromatography-Electron-Capture Negative Ion Mass Spectrometry (GC-ECNI-MS):
TTBB serves as an alternative to PFBB in electrophoric derivatization reactions prior to detection during GC-ECNI-MS. This application allows for the analysis of compounds that may be difficult to detect using traditional methods, providing a valuable tool for researchers in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 76437-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,3 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76437-40:
(7*7)+(6*6)+(5*4)+(4*3)+(3*7)+(2*4)+(1*0)=146
146 % 10 = 6
So 76437-40-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H2BrF7/c9-1-2-4(10)6(12)3(8(14,15)16)7(13)5(2)11/h1H2

76437-40-6 Well-known Company Product Price

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  • Aldrich

  • (406406)  2,3,5,6-Tetrafluoro-4-(trifluoromethyl)benzylbromide  98%

  • 76437-40-6

  • 406406-1G

  • 1,085.76CNY

  • Detail

76437-40-6SDS

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 4-(Bromomethyl)-2,3,5,6-tetrafluoro-benzotrifluoride

1.2 Other means of identification

Product number -
Other names 2,3,5,6-TETRAFLUORO-4-(TRIFLUOROMETHYL)BENZYL BROMIDE

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:76437-40-6 SDS

76437-40-6Downstream Products

76437-40-6Relevant academic research and scientific papers

New preparation method of 1-bromo-methyl-2,3,5,6-tetrafluoro-4-(trifluoromethyl)benzene

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Paragraph 0034; 0044-0045; 0089-0091; 0092-0097, (2019/08/20)

The invention discloses a new preparation method of 1-bromo-methyl-2,3,5,6-tetrafluoro-4-(trifluoromethyl)benzene. The method comprises the steps that with a compound 2,3,5,6-tetrafluoro-terephthalicacid as a raw material, through alkylation, 2,3,5,6-tetrafluoro-terephthalic acid diester is obtained firstly, then single hydrolysis is conducted, formic acid is fluorinated into trifluoromethyl so as to obtain 2,3,5,6-tetrafluoro-4-trifluoromethyl benzoate, and after the 2,3,5,6-tetrafluoro-4-trifluoromethyl benzoate is reduced into alcohol, through bromination, the target compound is obtained.According to the method, the reaction raw materials are easy to obtain and low in price, few reaction by-products are generated, and the product is easy to purify, high in yield and suitable for massindustrial production; therefore, reliable guarantee is provided for a key intermediate of a novel drug 2-hydroxyl-5-(2,3,5,6-tetrafluoro-4-trifluoromethyl benzylamino)benzoic acid.

Halogenated esters

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, (2008/06/13)

Compounds of formula I wherein R1 and R2 are each selected from halomethyl and halo and R is nitro, cyano, lower alkoxycarbonyl, lower alkylcarbonyl, or di- or trifluoromethyl, and n has a value of zero to four, and compositions comprising them are useful as insecticides in agriculture, horticulture and other outlets. They may optionally be combined with other pesticides and/or synergists. The compounds may be prepared by conventional esterification processes from the corresponding acids and appropriately substituted benzyl alcohols or halides, some of which are novel. STR1

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