Cas 80851-20-3,(3S,4S,5S,6R,8S)-1-Methyl-2,7,9,10-tetraoxa-tricyclo[4.3.2.0<sup>3,8</sup>]undecane-4,5-diol

80851-20-3

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Basic information

Product Name: (3S,4S,5S,6R,8S)-1-Methyl-2,7,9,10-tetraoxa-tricyclo[4.3.2.0^3,8]undecane-4,5-diol
Synonyms:
CAS NO:80851-20-3
Molecular Formula:
Molecular Weight: 204.18
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: (3S,4S,5S,6R,8S)-1-Methyl-2,7,9,10-tetraoxa-tricyclo[4.3.2.0^3,8]undecane-4,5-diol(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4S,5S,6R,8S)-1-Methyl-2,7,9,10-tetraoxa-tricyclo[4.3.2.0^3,8]undecane-4,5-diol(80851-20-3)
EPA Substance Registry System: (3S,4S,5S,6R,8S)-1-Methyl-2,7,9,10-tetraoxa-tricyclo[4.3.2.0^3,8]undecane-4,5-diol(80851-20-3)

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: 80851-20-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 80851-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,5 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80851-20:
(7*8)+(6*0)+(5*8)+(4*5)+(3*1)+(2*2)+(1*0)=123
123 % 10 = 3
So 80851-20-3 is a valid CAS Registry Number.

80851-20-3Upstream product

76985-96-1 3,4,6-tri-O-acetyl-1,2-O-(1-(exo-p-tolylthio)ethylidene)-beta-D-mannopyranose

80851-20-3Downstream Products

80851-20-3Relevant academic research and scientific papers

REACTIONS OF SUGAR THIO-ORTHOESTERS: NUCLEOPHILIC SUBSTITUTION OF AN ARYLTHIO GROUP DURING ZEMPLEN DEACYLATION

Backinowsky, Leon V.,Byramova, Narguiz E.,Tsvetkov, Yury E.,Betaneli, Vitali I.

, p. 181 - 194 (2007/10/02)

Deacylation of acetylated and benzoylated sugar 1,2-thio-orthoesters bearing an S-aromatic residue with methanolic sodium methoxide is accompanied by inter- and intra-molecular nucleophilic substitution of the arylthio group with formation of the correspo

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