Cas 1064157-06-7,methyl (5S)-1,2,3,5,6,7-hexahydro-3-(9-tert-butyldiphenylsilyloxynonyl)-5-hydroxy-1-thioxo-pyrrolo[1,2-c]pyrimidine-4-carboxylate

1064157-06-7

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Basic information

Product Name: methyl (5S)-1,2,3,5,6,7-hexahydro-3-(9-tert-butyldiphenylsilyloxynonyl)-5-hydroxy-1-thioxo-pyrrolo[1,2-c]pyrimidine-4-carboxylate
Synonyms:
CAS NO:1064157-06-7
Molecular Formula:
Molecular Weight: 608.918
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: methyl (5S)-1,2,3,5,6,7-hexahydro-3-(9-tert-butyldiphenylsilyloxynonyl)-5-hydroxy-1-thioxo-pyrrolo[1,2-c]pyrimidine-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (5S)-1,2,3,5,6,7-hexahydro-3-(9-tert-butyldiphenylsilyloxynonyl)-5-hydroxy-1-thioxo-pyrrolo[1,2-c]pyrimidine-4-carboxylate(1064157-06-7)
EPA Substance Registry System: methyl (5S)-1,2,3,5,6,7-hexahydro-3-(9-tert-butyldiphenylsilyloxynonyl)-5-hydroxy-1-thioxo-pyrrolo[1,2-c]pyrimidine-4-carboxylate(1064157-06-7)

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1064157-06-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1064157-06-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,4,1,5 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1064157-06:
(9*1)+(8*0)+(7*6)+(6*4)+(5*1)+(4*5)+(3*7)+(2*0)+(1*6)=127
127 % 10 = 7
So 1064157-06-7 is a valid CAS Registry Number.

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1064157-06-7Relevant academic research and scientific papers

A concise diastereoselective approach to the left-hand side of batzelladine A

Davies, Christopher D.,Elliott, Mark C.,Hill-Cousins, Joseph,Khan, Misbah-Ul A.,Maqbool, Tahir,Wood, John L.

, p. 2028 - 2032 (2008)

A highly diastereoselective three-component coupling reaction has been used in a concise approach to the left-hand side of batzelladine A. The stereoselectivity of this reaction, along with related observations described herein, provides insight into the mechanism of this reaction.

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