Cas 1133159-34-8,p-tolyl 4-O-acetyl-2-O-benzoyl-3-bromo-3,6-dideoxy-1-thio-α-D-altropyranoside

1133159-34-8

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Basic information

Product Name: p-tolyl 4-O-acetyl-2-O-benzoyl-3-bromo-3,6-dideoxy-1-thio-α-D-altropyranoside
Synonyms: p-tolyl 4-O-acetyl-2-O-benzoyl-3-bromo-3,6-dideoxy-1-thio-α-D-altropyranoside
CAS NO:1133159-34-8
Molecular Formula:
Molecular Weight: 479.392
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: p-tolyl 4-O-acetyl-2-O-benzoyl-3-bromo-3,6-dideoxy-1-thio-α-D-altropyranoside(CAS DataBase Reference)
NIST Chemistry Reference: p-tolyl 4-O-acetyl-2-O-benzoyl-3-bromo-3,6-dideoxy-1-thio-α-D-altropyranoside(1133159-34-8)
EPA Substance Registry System: p-tolyl 4-O-acetyl-2-O-benzoyl-3-bromo-3,6-dideoxy-1-thio-α-D-altropyranoside(1133159-34-8)

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: 1133159-34-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1133159-34-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,3,1,5 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1133159-34:
(9*1)+(8*1)+(7*3)+(6*3)+(5*1)+(4*5)+(3*9)+(2*3)+(1*4)=118
118 % 10 = 8
So 1133159-34-8 is a valid CAS Registry Number.

1133159-34-8Upstream product

106-45-6 para-thiocresol

1133159-34-8Downstream Products

1133159-40-6 p-tolyl 2,3-anhydro-1-thio-α-D-rhamnopyranoside

1133159-34-8Relevant academic research and scientific papers

2,3-Anhydrosugars in glycoside bond synthesis. Application to 2,6-dideoxypyranosides

Hou, Dianjie,Lowary, Todd L.

experimental part, p. 2278 - 2289 (2009/08/07)

We describe here the first use of 2,3-anhydrosugars as glycosylating agents for the preparation of 2-deoxypyranosides. In particular, the methodology was used to assemble 2,6-dideoxysugar glycosides. Glycosylation of a panel of alcohols with one of two 6-

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