Cas 139924-63-3,methyl 2,3-di-O-acetyl-4-O-benzoyl-6-deoxy-3-C-methyl-α-D-glucopyranoside

139924-63-3

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Basic information

Product Name: methyl 2,3-di-O-acetyl-4-O-benzoyl-6-deoxy-3-C-methyl-α-D-glucopyranoside
Synonyms: methyl 2,3-di-O-acetyl-4-O-benzoyl-6-deoxy-3-C-methyl-α-D-glucopyranoside
CAS NO:139924-63-3
Molecular Formula:
Molecular Weight: 380.395
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 2,3-di-O-acetyl-4-O-benzoyl-6-deoxy-3-C-methyl-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2,3-di-O-acetyl-4-O-benzoyl-6-deoxy-3-C-methyl-α-D-glucopyranoside(139924-63-3)
EPA Substance Registry System: methyl 2,3-di-O-acetyl-4-O-benzoyl-6-deoxy-3-C-methyl-α-D-glucopyranoside(139924-63-3)

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: 139924-63-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 139924-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,9,2 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 139924-63:
(8*1)+(7*3)+(6*9)+(5*9)+(4*2)+(3*4)+(2*6)+(1*3)=163
163 % 10 = 3
So 139924-63-3 is a valid CAS Registry Number.

139924-63-3Upstream product

132602-79-0 methyl 2,3-di-O-acetyl-4-O-benzoyl-6-bromo-6-deoxy-3-C-methyl-α-D-glucopyranoside

139924-63-3Downstream Products

139924-63-3Relevant academic research and scientific papers

Stereoselectivities in Catalytic Hydrogenation of Several Branched-Chain 6-Deoxyhex-5-enopyranosides. A Synthesis of Branched-Chain Methyl 6-Deoxy-β-L-hexopyranoside

Sato, Ken-ichi,Sakuma, Shogo,Takahashi, Kazuo,Hashimoto, Hironobu

, p. 292 - 294 (1992)

Hydrogenation of several 2-C-, 3-C-, and 4-C-methyl-branched-6-deoxyhex-5-enopyranosides in the presence of palladium-carbon in ethanol showed stereoselective formation of the corresponding 6-deoxy-β-L-hexopyranosides.

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