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1202405-84-2

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1202405-84-2 Usage

General Description

2,5-Pyrrolidinedione, 3,3,4,4-tetramethyl-1-(7-methyl-3H-imidazo[4,5-c]pyridin-4-yl)- is a chemical compound with a complex molecular structure. It contains a pyrrolidinedione ring and a tetramethyl-1-7-methyl-3H-imidazo[4,5-c]pyridin-4-yl group. 2,5-Pyrrolidinedione, 3,3,4,4-tetramethyl-1-(7-methyl-3H-imidazo[4,5-c]pyridin-4-yl)- is potentially used in pharmaceutical research and drug development due to its unique structure and potential biological activity. Its specific properties and potential applications would need to be further investigated and studied.

Check Digit Verification of cas no

The CAS Registry Mumber 1202405-84-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,4,0 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1202405-84:
(9*1)+(8*2)+(7*0)+(6*2)+(5*4)+(4*0)+(3*5)+(2*8)+(1*4)=92
92 % 10 = 2
So 1202405-84-2 is a valid CAS Registry Number.

1202405-84-2SDS

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 N-(7-methyl-1H-imidazo[4,5-c]pyridin-4-yl)-2,2,3,3-tetramethylsuccinimide

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:1202405-84-2 SDS

1202405-84-2Relevant articles and documents

Tetramethylsuccinimide as a directing/protecting group in purine glycosylates

Arico, Joseph W.,Calhoun, Amy K.,Salandria, Kerry J.,McLaughlin, Larry W.

supporting information; experimental part, p. 120 - 122 (2010/05/18)

Chemical Equation Presented Tetramethylsuccinic anhydride can be used to protect the exocyclic amine of 6-aminopurine derivatives by forming the corresponding tetramethysuccinimide. X-ray crystallography confirms that the imide carbonyl and the methyl groups are positioned to sterically block the N7 nitrogen so that glycosylations occur with very high regiochemical control at N9. This approach is particularly effective for 3-substituted purines where the substituent tends to block access to N9 and inhibit glycosylation at that site.

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