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3-bromo-N-[2-methyl-5-([1,3]oxazolo[4,5-b]pyridin-2-yl)phenyl]benzamide is a complex organic compound with a molecular formula of C20H14BrN3O2. It is characterized by the presence of a bromo group (Br), a benzamide group, and a substituted phenyl ring with a methyl group and a [1,3]oxazolo[4,5-b]pyridin-2-yl moiety. 3-bromo-N-[2-methyl-5-([1,3]oxazolo[4,5-b]pyridin-2-yl)phenyl]benzamide is a member of the benzamide class of chemicals, which are known for their potential applications in pharmaceuticals and agrochemicals. The specific structure of 3-bromo-N-[2-methyl-5-([1,3]oxazolo[4,5-b]pyridin-2-yl)phenyl]benzamide, with its unique arrangement of functional groups, suggests that it may have specific biological activities or properties that could be relevant in the development of new drugs or chemical intermediates.

5845-68-1

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5845-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5845-68-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5845-68:
(6*5)+(5*8)+(4*4)+(3*5)+(2*6)+(1*8)=121
121 % 10 = 1
So 5845-68-1 is a valid CAS Registry Number.

5845-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-N-[2-methyl-5-([1,3]oxazolo[4,5-b]pyridin-2-yl)phenyl]benzamide

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5845-68-1 SDS

5845-68-1Downstream Products

5845-68-1Relevant academic research and scientific papers

PHENACYL ESTERS OF AMINO ACIDS AND PEPTIDES

Popova, O. Yu.,Yung, R.,Mitin, Yu. V.

, p. 1499 - 1502 (2007/10/02)

The behavior of phenacyl esters under the conditions of peptide synthesis was investigated.The cleavage of phenacyl esters in reaction with primary amines, as a result of which the carboxyl group is liberated, was discovered.In the presence of lower alcohols the phenacyl esters can undergo transesterification.The phenacyl group is removed by treatment with zinc dust in mixtures of acetic acid with dimethylformamide or trifluoroethanol.

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