Cas 79526-61-7,Toluene-4-sulfonic acid (3aR,4S,6R,7R,7aS)-7-hydroxy-4-methoxy-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ylmethyl ester

79526-61-7

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Basic information

Product Name: Toluene-4-sulfonic acid (3aR,4S,6R,7R,7aS)-7-hydroxy-4-methoxy-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ylmethyl ester
Synonyms:
CAS NO:79526-61-7
Molecular Formula:
Molecular Weight: 360.385
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: Toluene-4-sulfonic acid (3aR,4S,6R,7R,7aS)-7-hydroxy-4-methoxy-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Toluene-4-sulfonic acid (3aR,4S,6R,7R,7aS)-7-hydroxy-4-methoxy-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ylmethyl ester(79526-61-7)
EPA Substance Registry System: Toluene-4-sulfonic acid (3aR,4S,6R,7R,7aS)-7-hydroxy-4-methoxy-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-ylmethyl ester(79526-61-7)

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: 79526-61-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 79526-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,5,2 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79526-61:
(7*7)+(6*9)+(5*5)+(4*2)+(3*6)+(2*6)+(1*1)=167
167 % 10 = 7
So 79526-61-7 is a valid CAS Registry Number.

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79526-61-7Relevant academic research and scientific papers

Branched-chain Sugars. XXII. Synthesis of Benzyl 2,3-Di-O-benzyl- and 2,3-O-Methylene-β-L-threo-pentopyranosid-4-uloses, and the Corresponding 6-Deoxy-α-D-xylo-hexopyranosid-4-uloses

Matsuzawa, Masafumi,Kubo, Kazusuke,Kodama, Hisashi

, p. 2169 - 2173 (1981)

The title compounds were synthesized from L-arabinose and D-glucose as intermediates to a few naturally occurring branched-chain sugars.Oxidation conditions of precursors to the corresponding 4-uloses were examined.

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