Cas 169048-75-3,methyl 6-S-acetyl-2,4-di-O-benzoyl-6-deoxy-3-O-methanesulfonyl-6-thio-α-D-glucopyranoside

169048-75-3

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Basic information

Product Name: methyl 6-S-acetyl-2,4-di-O-benzoyl-6-deoxy-3-O-methanesulfonyl-6-thio-α-D-glucopyranoside
Synonyms:
CAS NO:169048-75-3
Molecular Formula:
Molecular Weight: 538.596
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 6-S-acetyl-2,4-di-O-benzoyl-6-deoxy-3-O-methanesulfonyl-6-thio-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 6-S-acetyl-2,4-di-O-benzoyl-6-deoxy-3-O-methanesulfonyl-6-thio-α-D-glucopyranoside(169048-75-3)
EPA Substance Registry System: methyl 6-S-acetyl-2,4-di-O-benzoyl-6-deoxy-3-O-methanesulfonyl-6-thio-α-D-glucopyranoside(169048-75-3)

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: 169048-75-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 169048-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,0,4 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 169048-75:
(8*1)+(7*6)+(6*9)+(5*0)+(4*4)+(3*8)+(2*7)+(1*5)=163
163 % 10 = 3
So 169048-75-3 is a valid CAS Registry Number.

169048-75-3Upstream product

169048-75-3Downstream Products

31899-66-8 methyl 3,6-dideoxy-α-D-ribo-hexapyranoside

169048-75-3Relevant academic research and scientific papers

3,6-Thioanhydro sugars as important key intermediates in the enantiospecific synthesis of chiral polyhydroxythiolanes

Izquierdo,Plaza,Asenjo,Rodriguez

, p. 1117 - 1122 (2007/10/02)

Methyl 3,6-thioanhydro-α-D-glucopyranoside (5) was obtained in seven steps from the commercially available methyl α-D-glucopyranoside. Transformation of 5 into (2R,3R,4S)-3,4-dihydroxy-2-[(S)-1,2-dihydroxyethyl]thiolane (9) was achieved by acid hydrolysis

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