Cas 1166385-07-4,1β-[3-(carbamoyl)phenyl]-1-deoxy-2,3,5-tri-O-(tert-butyldimethyl-silyl)-D-ribofuranose

1166385-07-4

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Basic information

Product Name: 1β-[3-(carbamoyl)phenyl]-1-deoxy-2,3,5-tri-O-(tert-butyldimethyl-silyl)-D-ribofuranose
Synonyms: 1β-[3-(carbamoyl)phenyl]-1-deoxy-2,3,5-tri-O-(tert-butyldimethyl-silyl)-D-ribofuranose
CAS NO:1166385-07-4
Molecular Formula:
Molecular Weight: 596.043
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: 1β-[3-(carbamoyl)phenyl]-1-deoxy-2,3,5-tri-O-(tert-butyldimethyl-silyl)-D-ribofuranose(CAS DataBase Reference)
NIST Chemistry Reference: 1β-[3-(carbamoyl)phenyl]-1-deoxy-2,3,5-tri-O-(tert-butyldimethyl-silyl)-D-ribofuranose(1166385-07-4)
EPA Substance Registry System: 1β-[3-(carbamoyl)phenyl]-1-deoxy-2,3,5-tri-O-(tert-butyldimethyl-silyl)-D-ribofuranose(1166385-07-4)

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: 1166385-07-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1166385-07-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,6,3,8 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1166385-07:
(9*1)+(8*1)+(7*6)+(6*6)+(5*3)+(4*8)+(3*5)+(2*0)+(1*7)=164
164 % 10 = 4
So 1166385-07-4 is a valid CAS Registry Number.

1166385-07-4Upstream product

1166385-07-4Downstream Products

138385-29-2 [3H]-Benzamide riboside

1166385-07-4Relevant academic research and scientific papers

Synthesis of benzamide-C-ribonucleosides by Pd-catalyzed aminocarbonylations

?tefko, Martin,Pohl, Radek,Hocek, Michal

, p. 4471 - 4483 (2009)

A novel modular, efficient and practical methodology for preparation of p- and m-substituted benzamide-C-ribonucleosides was developed. Reaction of TBS-protected 3- and 4-bromophenyl-C-ribonucleosides 1 and 4 with various primary and secondary amines or N

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