Cas 470456-74-7,4-O-acetyl-3-O-(4-O-acetyl-6-bromo-2,6-dideoxy-2-thiophenyl-β-D-glucopyranosyl)-6-bromo-2,6-dideoxy-D-arabino-hex-1-enitol

470456-74-7

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Basic information

Product Name: 4-O-acetyl-3-O-(4-O-acetyl-6-bromo-2,6-dideoxy-2-thiophenyl-β-D-glucopyranosyl)-6-bromo-2,6-dideoxy-D-arabino-hex-1-enitol
Synonyms: 4-O-acetyl-3-O-(4-O-acetyl-6-bromo-2,6-dideoxy-2-thiophenyl-β-D-glucopyranosyl)-6-bromo-2,6-dideoxy-D-arabino-hex-1-enitol
CAS NO:470456-74-7
Molecular Formula:
Molecular Weight: 610.318
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: 4-O-acetyl-3-O-(4-O-acetyl-6-bromo-2,6-dideoxy-2-thiophenyl-β-D-glucopyranosyl)-6-bromo-2,6-dideoxy-D-arabino-hex-1-enitol(CAS DataBase Reference)
NIST Chemistry Reference: 4-O-acetyl-3-O-(4-O-acetyl-6-bromo-2,6-dideoxy-2-thiophenyl-β-D-glucopyranosyl)-6-bromo-2,6-dideoxy-D-arabino-hex-1-enitol(470456-74-7)
EPA Substance Registry System: 4-O-acetyl-3-O-(4-O-acetyl-6-bromo-2,6-dideoxy-2-thiophenyl-β-D-glucopyranosyl)-6-bromo-2,6-dideoxy-D-arabino-hex-1-enitol(470456-74-7)

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: 470456-74-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 470456-74-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,0,4,5 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 470456-74:
(8*4)+(7*7)+(6*0)+(5*4)+(4*5)+(3*6)+(2*7)+(1*4)=157
157 % 10 = 7
So 470456-74-7 is a valid CAS Registry Number.

470456-74-7Upstream product

470456-74-7Downstream Products

470456-75-8 4-O-acetyl-3-O-[4-O-acetyl-3-O-(3-O-acetyl-4-azido-2,4,6-trideoxy-α-L-glucopyranosyl)-6-bromo-2,6-dideoxy-2-thiophenyl-β-D-glucopyranosyl]-6-bromo-2,6-dideoxy-D-arabino-hex-1-enitol

470456-74-7Relevant academic research and scientific papers

Towards the synthesis of aureolic acid analogue conjugates: Synthesis and glycosidation reactions of 3-o-acetyl-4-azido-2,4,6-trideoxy-L-glucopyranose derivatives

Roush, William R.,James, Ray A.

, p. 141 - 146 (2002)

A stereoselective synthesis of 3-O-acetyl-4-azido-glucopyranose (6) is described. The derived anomeric acetate (13), and especially the thioglycoside (14), are demonstrated to be good donors for synthesis of α-glycosides of (6). Donor (14) was used in the

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