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3-cyano-2,6-dibromo-4-methylpyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38824-75-8

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38824-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38824-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,2 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38824-75:
(7*3)+(6*8)+(5*8)+(4*2)+(3*4)+(2*7)+(1*5)=148
148 % 10 = 8
So 38824-75-8 is a valid CAS Registry Number.

38824-75-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-cyano-2,6-dibromo-4-methylpyridine

1.2 Other means of identification

Product number -
Other names 2,6-dibromo-4-methylpyridine-3-carbonitrile

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:38824-75-8 SDS

38824-75-8Downstream Products

38824-75-8Relevant academic research and scientific papers

Facile and efficient synthesis of 4-alkyl derivatives of 3-carbamoyl- and 3,5-dicarbamoylpyridines as nicotinamide mimetics

Di Rienzo, Barbara,Mellini, Paolo,Tortorella, Silvano,De Vita, Daniela,Scipione, Luigi

, p. 3835 - 3838 (2010)

Nicotinamide plays a key role in many biological processes and, as a consequence, its derivatives could be attractive for the synthesis of biologically active compounds. Here a rapid and efficient way of preparing alkyl derivatives of nicotinamide, precisely, 4-alkyl-3-carbamoylpyridine and 4-alkyl-3,5-dicarbamoylpyridine is reported. The synthetic route developed adopts mild reaction conditions and produces target compounds in higher yields compared with methods described in literature. Georg Thieme Verlag Stuttgart · New York.

SOLUBLE FORMS OF INCLUSION COMPLEXES OF HISTONE DEACETYLASE INHIBITORS AND CYCLODEXTRINS, THEIR PREPARATION PROCESSES AND USES IN THE PHARMACEUTICAL FIELD

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Page/Page column 22; 23, (2008/12/07)

The invention relates to the preparation of soluble forms of complexes of histone deacetylase inhibitors and cyclodextrins. The preparation process involves the formation of inclusion complexes with cyclodextrins with the aid of microwaves. Their use is in the pharmaceutical field.

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