Cas 81562-15-4,L-1,3,4-tri-O-benzyl-5,6-O-cyclohexylidene-chiro-inositol 2-(S-methyl dithiocarbonate)

81562-15-4

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Basic information

Product Name: L-1,3,4-tri-O-benzyl-5,6-O-cyclohexylidene-chiro-inositol 2-(S-methyl dithiocarbonate)
Synonyms: L-1,3,4-tri-O-benzyl-5,6-O-cyclohexylidene-chiro-inositol 2-(S-methyl dithiocarbonate)
CAS NO:81562-15-4
Molecular Formula:
Molecular Weight: 620.831
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: L-1,3,4-tri-O-benzyl-5,6-O-cyclohexylidene-chiro-inositol 2-(S-methyl dithiocarbonate)(CAS DataBase Reference)
NIST Chemistry Reference: L-1,3,4-tri-O-benzyl-5,6-O-cyclohexylidene-chiro-inositol 2-(S-methyl dithiocarbonate)(81562-15-4)
EPA Substance Registry System: L-1,3,4-tri-O-benzyl-5,6-O-cyclohexylidene-chiro-inositol 2-(S-methyl dithiocarbonate)(81562-15-4)

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: 81562-15-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 81562-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,6 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 81562-15:
(7*8)+(6*1)+(5*5)+(4*6)+(3*2)+(2*1)+(1*5)=124
124 % 10 = 4
So 81562-15-4 is a valid CAS Registry Number.

81562-15-4Upstream product

81562-15-4Downstream Products

81562-16-5 D-1,2,5-tri-O-benzyl-3,4-O-cyclohexylidene-1,3,4/2,5-cyclohexanepentol

81562-15-4Relevant academic research and scientific papers

THE PREPARATION OF CYCLOHEXANEPENTOLS FROM INOSITOLS BY DEOXYGENATION

Angyal, Stephen J.,Odier, Leon

, p. 209 - 220 (2007/10/02)

Several cyclohexapenetols heva been synthesized from inositols by blocking all but one hydroxyl group, converting the free hydroxyl group into its S-methyl dithiocarbonate, and treating it with tributylstannane.Suitable blocking-groups are methyl, benzyl, and methylthiomethyl ethers, and acetals.One cyclohexanepentol was prepared by the reductive deamination of an aminodeoxyinositol.

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