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4-BroMoMethyl-2,6-diMethyl-pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79313-02-3

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79313-02-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79313-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,1 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79313-02:
(7*7)+(6*9)+(5*3)+(4*1)+(3*3)+(2*0)+(1*2)=133
133 % 10 = 3
So 79313-02-3 is a valid CAS Registry Number.

79313-02-3SDS

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 4-(bromomethyl)-2,6-dimethylpyridine

1.2 Other means of identification

Product number -
Other names 4-bromomethyl-2,6-lutidine

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:79313-02-3 SDS

79313-02-3Downstream Products

79313-02-3Relevant academic research and scientific papers

Synthesis of some fluorinated pyridines using tetrabutylammonium fluoride

Mobinikhaledi,Foroughifar

, p. 405 - 412 (2006)

Some bromo- and chloromethyl pyridines were synthesized using radical substitution reactions. Further reaction of these halopyridines with activated tetrabutylammonium fluoride under mild conditions gave the related fluorinated pyridines. The yields of products following recrystallization were of the order of 30-93%. 1H, 13C, and 19F spectroscopies together with elemental analysis were used characterize products. Copyright Taylor & Francis Group, LLC.

PROCESS FOR PREPARATION OF OPTICALLY ENRICHED ISOXAZOLINES

-

, (2021/10/11)

The invention relates to a process for preparing optically enriched isoxazoline compounds of formula (I), formula (I), wherein the variables are as defined in the specification, and the shown enantiomer has at least 55% ee; by oxo-Michael addition of hydr

N-SULFONYLPIPERIDINES AS METALLOPROTEINASE INHIBITORS (TACE)

-

Page/Page column 79, (2010/02/06)

Compounds of formula (1), wherein Z is -CONR15OH or -N(OH)CHO and X is -(CR9R10)t-Q-(CR11R12)u- (where t and u are independently 0 or 1 with the proviso that t and u cannot both be 0);are inhibitors o

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