Cas 64993-84-6,1-[O3,O5-bis-(4-methyl-benzoyl)-β-D-erythro-2-deoxy-pentofuranosyl]-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester

64993-84-6

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Basic information

Product Name: 1-[O³,O⁵-bis-(4-methyl-benzoyl)-β-D-erythro-2-deoxy-pentofuranosyl]-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester
Synonyms:
CAS NO:64993-84-6
Molecular Formula:
Molecular Weight: 493.516
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-[O³,O⁵-bis-(4-methyl-benzoyl)-β-D-erythro-2-deoxy-pentofuranosyl]-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-[O³,O⁵-bis-(4-methyl-benzoyl)-β-D-erythro-2-deoxy-pentofuranosyl]-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester(64993-84-6)
EPA Substance Registry System: 1-[O³,O⁵-bis-(4-methyl-benzoyl)-β-D-erythro-2-deoxy-pentofuranosyl]-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester(64993-84-6)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 64993-84-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 64993-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,9 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64993-84:
(7*6)+(6*4)+(5*9)+(4*9)+(3*3)+(2*8)+(1*4)=176
176 % 10 = 6
So 64993-84-6 is a valid CAS Registry Number.

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64993-84-6Relevant academic research and scientific papers

A highly efficient microwave-assisted solvent-free synthesis of α- and β-2′-deoxy-1,2,3-triazolyl-nucleosides

Guezguez, Raja,Bougrin, Khalid,El Akri, Khalid,Benhida, Rachid

, p. 4807 - 4811 (2006)

Microwave activation coupled with Cu(I) catalysis, under solvent-free conditions, was found to dramatically enhance the 1,3-dipolar cycloaddition between azido-2′-deoxyribose and terminal alkynes. The process is highly efficient and quantitatively affords

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