Cas 73793-22-3,1'-O-Benzyl-4',6'-O-benzyliden-2'-desoxy-2-methyl-α-D-allopyranosido<2',3':4,5>-2-oxazolin

73793-22-3

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Basic information

Product Name: 1'-O-Benzyl-4',6'-O-benzyliden-2'-desoxy-2-methyl-α-D-allopyranosido<2',3':4,5>-2-oxazolin
Synonyms: 1'-O-Benzyl-4',6'-O-benzyliden-2'-desoxy-2-methyl-α-D-allopyranosido<2',3':4,5>-2-oxazolin
CAS NO:73793-22-3
Molecular Formula:
Molecular Weight: 381.428
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'-O-Benzyl-4',6'-O-benzyliden-2'-desoxy-2-methyl-α-D-allopyranosido<2',3':4,5>-2-oxazolin(CAS DataBase Reference)
NIST Chemistry Reference: 1'-O-Benzyl-4',6'-O-benzyliden-2'-desoxy-2-methyl-α-D-allopyranosido<2',3':4,5>-2-oxazolin(73793-22-3)
EPA Substance Registry System: 1'-O-Benzyl-4',6'-O-benzyliden-2'-desoxy-2-methyl-α-D-allopyranosido<2',3':4,5>-2-oxazolin(73793-22-3)

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: 73793-22-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 73793-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,9 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 73793-22:
(7*7)+(6*3)+(5*7)+(4*9)+(3*3)+(2*2)+(1*2)=153
153 % 10 = 3
So 73793-22-3 is a valid CAS Registry Number.

73793-22-3Upstream product

13343-65-2 Benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-methanesulfonyl-α-D-glucopyranoside

73793-22-3Downstream Products

73793-22-3Relevant academic research and scientific papers

Di- and Polyamino Sugars, XXVIII. - Substitution Reactions of 2-Amino-2-deoxy-α-D-glucopyranosides at Position 3

Reckendorf, Wolfgang Meyer zu,Lenzen, Heinz-Juergen

, p. 265 - 274 (2007/10/02)

Nucleophilic substitutions of N-protected 2-amino-2-deoxy-3-O-mesyl-α-D-glucopyranosides with azide ions were severely restricted by neighboring group participations.N-acetyl as blocking group (2) led to the formation of the oxazoline 3 while from N-dinit

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