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329-97-5

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329-97-5 Usage

General Description

Benzyltrimethylammonium fluoride is a chemical compound with the formula C14H22F2N. It is commonly used as a reagent in organic synthesis and as a catalyst in various chemical reactions. It is a fluorinating agent, meaning it is used to introduce fluorine atoms into organic molecules. Benzyltrimethylammonium fluoride is a soluble, crystalline solid that is often used in research laboratories as a source of fluoride ions. It is also used in pharmaceutical and agrochemical industries for the synthesis of various fluorine-containing compounds. Despite its usefulness as a reagent, benzyltrimethylammonium fluoride must be handled with caution as it is toxic if ingested or if it comes into contact with the skin and eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 329-97-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 329-97:
(5*3)+(4*2)+(3*9)+(2*9)+(1*7)=75
75 % 10 = 5
So 329-97-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H16N.FH/c1-11(2,3)9-10-7-5-4-6-8-10;/h4-8H,9H2,1-3H3;1H/q+1;/p-1

329-97-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzyltrimethylammonium fluoride

1.2 Other means of identification

Product number -
Other names BENZYLTRIMETHYLAMMONIUM FLUORIDE MONOHYDRATE

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:329-97-5 SDS

329-97-5Relevant articles and documents

Fluoride-Mediated Reactions of Enol Silyl Ethers. Regiospecific Monoalkylation of Ketones

Kuwajima, Isao,Nakamura, Eiichi,Shimizu, Makoto

, p. 1025 - 1030 (2007/10/02)

Treatment of enol silyl ethers with alkyl halides in the presence of benzyltrimethylammonium fluoride and molecular sieves at room temperature gives the corresponding monoalkylated products with high regiospecificity.In most cases no polyalkylated products formed in the reaction.The alkylation reaction is highly chemospecific: esters, epoxides, and even ketones survive the reaction conditions.The reactions of various cyclohexanone derivatives proceed with the preferential axial attack of the electrophile.

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