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3545-76-4

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3545-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3545-76-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,4 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3545-76:
(6*3)+(5*5)+(4*4)+(3*5)+(2*7)+(1*6)=94
94 % 10 = 4
So 3545-76-4 is a valid CAS Registry Number.

3545-76-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3',5'-cyclic IMP

1.2 Other means of identification

Product number -
Other names O3',O5'-hydroxyphosphoryl-inosine

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:3545-76-4 SDS

3545-76-4Upstream product

3545-76-4Downstream Products

3545-76-4Relevant articles and documents

AMP Deaminase as a Novel Practical Catalyst in the Synthesis of 6-Oxopurine Ribosides and Their Analogs

Margolin, Alexey L.,Borcherding, David R.,Wolf-Kugel, Dominique,Margolin, Nara

, p. 7214 - 7218 (1994)

Adenylic acid deaminase from Aspergillus niger (AMP deaminase; AMPDA; EC 3.5.4.6) has beenintroduced as a novel practical catalyst in the synthesis of 6-oxopurine riboside and their analogs.This enzyme has a very broad substrate specificity and has been used on a preparative scale for deamination of several derivatives of adenosine including phosphorylated, cyclic, carbocyclic as well as cyclic analogs.In addition, AMPDA catalyzes dechlorination and demethoxylation of the purine ribosides.Overall substrate specificity of AMPDA is much broader than that of adenosine deaminase which can also be used for the synthesis of 6-oxopurine ribosides.Although the stereoselectivity of AMPDA is modest, this enzyme has successfully been used in the synthesis of a novel antiviral agent, carbovir phosphonate (14), after the carbocyclic component was resolved via lipase-catalyzed hydrolysis or acylation.

Synthesis and biological activity of several 6-substituted 9-b-D-ribofuranosylpurine 3',5'-cyclic phosphates.

Meyer et al.

, p. 2704,2705 (2007/10/05)

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