Cas 121633-37-2,1,6-anhydro-2,4-di-O-benzyl-3-O-(S-methylthiocarbonyl)-β-D-glucopyranose

121633-37-2

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Basic information

Product Name: 1,6-anhydro-2,4-di-O-benzyl-3-O-(S-methylthiocarbonyl)-β-D-glucopyranose
Synonyms: 1,6-anhydro-2,4-di-O-benzyl-3-O-(S-methylthiocarbonyl)-β-D-glucopyranose
CAS NO:121633-37-2
Molecular Formula:
Molecular Weight: 432.562
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: 1,6-anhydro-2,4-di-O-benzyl-3-O-(S-methylthiocarbonyl)-β-D-glucopyranose(CAS DataBase Reference)
NIST Chemistry Reference: 1,6-anhydro-2,4-di-O-benzyl-3-O-(S-methylthiocarbonyl)-β-D-glucopyranose(121633-37-2)
EPA Substance Registry System: 1,6-anhydro-2,4-di-O-benzyl-3-O-(S-methylthiocarbonyl)-β-D-glucopyranose(121633-37-2)

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: 121633-37-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 121633-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,6,3 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 121633-37:
(8*1)+(7*2)+(6*1)+(5*6)+(4*3)+(3*3)+(2*3)+(1*7)=92
92 % 10 = 2
So 121633-37-2 is a valid CAS Registry Number.

121633-37-2Upstream product

121633-37-2Downstream Products

85028-66-6 1,6-anhydro-2,4-di-O-benzyl-3-deoxy-β-D-ribohexapyranose

121633-37-2Relevant academic research and scientific papers

PROSTANOIDS. LVI. USEFUL PROSTAGLANDIN SYNTHONS FROM LEVOGLUCOSAN

Tolstikov, G. A.,Valeev, F. A.,Ibragimova, I. P.,Gaisina, I. N.,Spirikhin, L. V.,Miftakhov, M. S.

, p. 1501 - 1506 (2007/10/02)

(1S,6S,7R,9R)-7,9-Dihydroxy-3-oxabicyclononan-4-one, which is a new chiral synthon for cyclopentanoids, was obtained by intramolecular radical cyclization of methyl 4R,6S-dibenzyloxy-7R-hydroxy-8-acetoxyoct-2E,Z-enoates and subsequent removal of th

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