Cas 96445-98-6,2-<(5-amino-6,7-dihydro-7-oxo-3H-1,2,3-triazolo<4,5-d>pyrimidin-3-yl)methoxy>ethyl benzoate

96445-98-6

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Basic information

Product Name: 2-<(5-amino-6,7-dihydro-7-oxo-3H-1,2,3-triazolo<4,5-d>pyrimidin-3-yl)methoxy>ethyl benzoate
Synonyms: 2-<(5-amino-6,7-dihydro-7-oxo-3H-1,2,3-triazolo<4,5-d>pyrimidin-3-yl)methoxy>ethyl benzoate
CAS NO:96445-98-6
Molecular Formula:
Molecular Weight: 330.303
EINECS: N/A
Product Categories: N/A
Mol File: 96445-98-6.mol
Article Data: 2

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: 2-<(5-amino-6,7-dihydro-7-oxo-3H-1,2,3-triazolo<4,5-d>pyrimidin-3-yl)methoxy>ethyl benzoate(CAS DataBase Reference)
NIST Chemistry Reference: 2-<(5-amino-6,7-dihydro-7-oxo-3H-1,2,3-triazolo<4,5-d>pyrimidin-3-yl)methoxy>ethyl benzoate(96445-98-6)
EPA Substance Registry System: 2-<(5-amino-6,7-dihydro-7-oxo-3H-1,2,3-triazolo<4,5-d>pyrimidin-3-yl)methoxy>ethyl benzoate(96445-98-6)

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: 96445-98-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 96445-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,4,4 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96445-98:
(7*9)+(6*6)+(5*4)+(4*4)+(3*5)+(2*9)+(1*8)=176
176 % 10 = 6
So 96445-98-6 is a valid CAS Registry Number.

96445-98-6Upstream product

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96445-98-6Relevant articles and documents

Modifications on the Heterocyclic Base of Acyclovir: Syntheses and Antiviral Properties

Beauchamp, Lilia M.,Dolmatch, Bart L.,Schaeffer, Howard J.,Collins, Peter,Bauer, D. J.,et al.

, p. 982 - 987 (2007/10/02)

A griup of compounds were prepared in which variations of the ring portion of the acyclovir (ACV) structure were made.These modifications included monocyclic (isocytosine, triazole, imidazole), bicyclic (8-azapurine, pyrrolo pyrimidine, pyrazolo3,

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