Cas 824410-30-2,methyl 2,3-di-O-acetyl-4-C-[(S)-1-O-hydroxy-1-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)-methyl]-4,6-dideoxy-α-D-arabino-hex-5-enopyranoside

824410-30-2

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Basic information

Product Name: methyl 2,3-di-O-acetyl-4-C-[(S)-1-O-hydroxy-1-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)-methyl]-4,6-dideoxy-α-D-arabino-hex-5-enopyranoside
Synonyms:
CAS NO:824410-30-2
Molecular Formula:
Molecular Weight: 796.912
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-C-[(S)-1-O-hydroxy-1-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)-methyl]-4,6-dideoxy-α-D-arabino-hex-5-enopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2,3-di-O-acetyl-4-C-[(S)-1-O-hydroxy-1-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)-methyl]-4,6-dideoxy-α-D-arabino-hex-5-enopyranoside(824410-30-2)
EPA Substance Registry System: methyl 2,3-di-O-acetyl-4-C-[(S)-1-O-hydroxy-1-(2',3',4',6'-tetra-O-benzyl-β-D-glucopyranosyl)-methyl]-4,6-dideoxy-α-D-arabino-hex-5-enopyranoside(824410-30-2)

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: 824410-30-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 824410-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,4,4,1 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 824410-30:
(8*8)+(7*2)+(6*4)+(5*4)+(4*1)+(3*0)+(2*3)+(1*0)=132
132 % 10 = 2
So 824410-30-2 is a valid CAS Registry Number.

824410-30-2Upstream product

824410-14-2 methyl 6-bromo-4,6-dideoxy-α-D-threo-hex-4-enopyranoside

824410-30-2Downstream Products

824410-30-2Relevant academic research and scientific papers

Indium-promoted Barbier-type allylations in aqueous media: A convenient approach to 4-C-branched monosaccharides and (1→4)-C-disaccharides

Levoirier, Eric,Canac, Yves,Norsikian, Stéphanie,Lubineau, André

, p. 2737 - 2747 (2007/10/03)

Starting from methyl 6-bromo-4,6-dideoxy-α-d-threo-4-enopyranoside, 4-C-branched sugars have been prepared through indium-promoted Barbier-type allylation of various aldehydes in aqueous media followed by hydroboration of the resulting double bond. The intermediate unsaturated monosaccharides were shown to rearrange in acidic media to give 4-C-acetyl-5-C-alkyl pyranose compounds. From β-1-formyl sugars the corresponding β-(1→4)-C- disaccharides were obtained.

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