Cas 925672-08-8,(1S,2S,3R)-3-amino-4-[2,3-(isopropylidenedioxy)-4-(trityloxymethyl)-4-cyclopenten-1-yl]-1H-pyrrole-2-carboxylic acid ethyl ester

925672-08-8

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Basic information

Product Name: (1S,2S,3R)-3-amino-4-[2,3-(isopropylidenedioxy)-4-(trityloxymethyl)-4-cyclopenten-1-yl]-1H-pyrrole-2-carboxylic acid ethyl ester
Synonyms:
CAS NO:925672-08-8
Molecular Formula:
Molecular Weight: 564.681
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: (1S,2S,3R)-3-amino-4-[2,3-(isopropylidenedioxy)-4-(trityloxymethyl)-4-cyclopenten-1-yl]-1H-pyrrole-2-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,3R)-3-amino-4-[2,3-(isopropylidenedioxy)-4-(trityloxymethyl)-4-cyclopenten-1-yl]-1H-pyrrole-2-carboxylic acid ethyl ester(925672-08-8)
EPA Substance Registry System: (1S,2S,3R)-3-amino-4-[2,3-(isopropylidenedioxy)-4-(trityloxymethyl)-4-cyclopenten-1-yl]-1H-pyrrole-2-carboxylic acid ethyl ester(925672-08-8)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 925672-08-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 925672-08-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,5,6,7 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 925672-08:
(8*9)+(7*2)+(6*5)+(5*6)+(4*7)+(3*2)+(2*0)+(1*8)=188
188 % 10 = 8
So 925672-08-8 is a valid CAS Registry Number.

925672-08-8Upstream product

925672-08-8Downstream Products

925672-09-9 9-[(1S,2S,3R)-2,3-(isopropylidenedioxy)-4-(trityloxymethyl)-4-cyclopenten-1-yl]-9-deazaguanosine

925672-08-8Relevant academic research and scientific papers

Enantioselective synthesis and antiviral activity of purine and pyrimidine cyclopentenyl C-nucleosides

Rao, Jagadeeshwar R.,Schinazi, Raymond F.,Chu, Chung K.

, p. 839 - 846 (2007)

The enantiomerically pure carbocyclic purine and pyrimidine C-nucleosides 1-4 were synthesized via the key intermediate, 2,3-(isopropylidenedioxy)-4-(trityloxymethyl)-4-cyclopenten-1-ol (5), which was prepared from d-ribose in eight steps. Synthesized com

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