Cas 63593-15-7,benzyl 2-acetamido-4,6-O-benzylidene-2,3-dideoxy-3-C-formyl-α-D-erythro-hex-2-enopyranoside

63593-15-7

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Basic information

Product Name: benzyl 2-acetamido-4,6-O-benzylidene-2,3-dideoxy-3-C-formyl-α-D-erythro-hex-2-enopyranoside
Synonyms: benzyl 2-acetamido-4,6-O-benzylidene-2,3-dideoxy-3-C-formyl-α-D-erythro-hex-2-enopyranoside
CAS NO:63593-15-7
Molecular Formula:
Molecular Weight: 409.439
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: benzyl 2-acetamido-4,6-O-benzylidene-2,3-dideoxy-3-C-formyl-α-D-erythro-hex-2-enopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 2-acetamido-4,6-O-benzylidene-2,3-dideoxy-3-C-formyl-α-D-erythro-hex-2-enopyranoside(63593-15-7)
EPA Substance Registry System: benzyl 2-acetamido-4,6-O-benzylidene-2,3-dideoxy-3-C-formyl-α-D-erythro-hex-2-enopyranoside(63593-15-7)

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: 63593-15-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 63593-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,9 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63593-15:
(7*6)+(6*3)+(5*5)+(4*9)+(3*3)+(2*1)+(1*5)=137
137 % 10 = 7
So 63593-15-7 is a valid CAS Registry Number.

63593-15-7Upstream product

62175-13-7 benzyl 2-acetamido-4,6-O-benzylidene-2,3-dideoxy-3-C-nitromethyl-α-D-erythro-hex-2-enopyranoside

63593-15-7Downstream Products

77453-60-2 benzyl 2-acetamido-4,6-O-benzylidene-2,3-dideoxy-3-C-hydroxymethyl-α-D-erythro-hex-2-enopyranoside

63593-15-7Relevant academic research and scientific papers

THE SYNTHESIS OF C-FORMYL, BRANCHED-CHAIN CARBOHYDRATE DERIVATIVES BY THE CONVERSION OF NITROMETHYL GROUPS INTO CARBONYL GROUPS

Nieuwenhuis, Jacobus J.,Jordaan, Johannes H.

, p. 185 - 192 (1980)

Addition of the sodium salts of five branched-chain nitromethyl sugars in N,N-dimethylformamide to aqueous solutions of titanium(III) chloride (at pH 1) produced the respective, C-formyl, branched-chain carbohydrate derivatives 3-C-formyl-1,2:5,6-di-O-iso

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