Cas 128364-98-7,5-(5-O-benzoyl-2,3-O-isopropylidene-β-D-ribofuranosyl)-1H-tetrazole

128364-98-7

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Basic information

Product Name: 5-(5-O-benzoyl-2,3-O-isopropylidene-β-D-ribofuranosyl)-1H-tetrazole
Synonyms: 5-(5-O-benzoyl-2,3-O-isopropylidene-β-D-ribofuranosyl)-1H-tetrazole
CAS NO:128364-98-7
Molecular Formula:
Molecular Weight: 346.343
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: 5-(5-O-benzoyl-2,3-O-isopropylidene-β-D-ribofuranosyl)-1H-tetrazole(CAS DataBase Reference)
NIST Chemistry Reference: 5-(5-O-benzoyl-2,3-O-isopropylidene-β-D-ribofuranosyl)-1H-tetrazole(128364-98-7)
EPA Substance Registry System: 5-(5-O-benzoyl-2,3-O-isopropylidene-β-D-ribofuranosyl)-1H-tetrazole(128364-98-7)

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: 128364-98-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128364-98-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,3,6 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 128364-98:
(8*1)+(7*2)+(6*8)+(5*3)+(4*6)+(3*4)+(2*9)+(1*8)=147
147 % 10 = 7
So 128364-98-7 is a valid CAS Registry Number.

128364-98-7Upstream product

29868-36-8 5-O-benzoyl-2,3-di-O-isopropylidene-β-D-ribofuranosyl-1-carbonitrile

128364-98-7Downstream Products

847386-37-2 2-phenyloxy-5-(5-O-benzoyl-2,3-O-isopropylidene-β-D-ribofuranosyl)-1,3,4-oxadiazole

128364-98-7Relevant academic research and scientific papers

Preparation and utility of 5-β-D-ribofuranosyl-1H-tetrazole as a key synthon for C-nucleoside synthesis

Kobe,Prhavc,Hohnjec,Townsend

, p. 2209 - 2244 (1994)

A synthesis of 5-β-D-ribofuranosyl-1H-tetrazole (2) and 5-β-D- ribofuranosyl-l,3,4-oxadiazole-2(3H)-one (9) derivatives is described. Ring transformations of 2 have been investigated in an effort to establish the stability of this synthon for further use

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