Cas 1310709-69-3,(4R)-4-benzyl-4-(4',6'-di-O-acetyl-2',3'-dideoxy-α-D-erythro-2'-hexenopyranosyl)-2-phenyl-5(4H)-oxazolone

1310709-69-3

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Basic information

Product Name: (4R)-4-benzyl-4-(4',6'-di-O-acetyl-2',3'-dideoxy-α-D-erythro-2'-hexenopyranosyl)-2-phenyl-5(4H)-oxazolone
Synonyms: (4R)-4-benzyl-4-(4',6'-di-O-acetyl-2',3'-dideoxy-α-D-erythro-2'-hexenopyranosyl)-2-phenyl-5(4H)-oxazolone
CAS NO:1310709-69-3
Molecular Formula:
Molecular Weight: 463.487
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: (4R)-4-benzyl-4-(4',6'-di-O-acetyl-2',3'-dideoxy-α-D-erythro-2'-hexenopyranosyl)-2-phenyl-5(4H)-oxazolone(CAS DataBase Reference)
NIST Chemistry Reference: (4R)-4-benzyl-4-(4',6'-di-O-acetyl-2',3'-dideoxy-α-D-erythro-2'-hexenopyranosyl)-2-phenyl-5(4H)-oxazolone(1310709-69-3)
EPA Substance Registry System: (4R)-4-benzyl-4-(4',6'-di-O-acetyl-2',3'-dideoxy-α-D-erythro-2'-hexenopyranosyl)-2-phenyl-5(4H)-oxazolone(1310709-69-3)

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: 1310709-69-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1310709-69-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,7,0 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1310709-69:
(9*1)+(8*3)+(7*1)+(6*0)+(5*7)+(4*0)+(3*9)+(2*6)+(1*9)=123
123 % 10 = 3
So 1310709-69-3 is a valid CAS Registry Number.

1310709-69-3Upstream product

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1310709-69-3Relevant academic research and scientific papers

Stereoselective Pd-catalyzed synthesis of quaternary α-d-C-mannosyl- (S)-amino acids

Di Giacomo, Marcello,Serra, Massimo,Brusasca, Marco,Colombo, Lino

, p. 5247 - 5257 (2011)

In this paper, we report the stereoselective synthesis of α-d-C-mannosyl-(S)-amino acids exploiting, as a key step, an allylic alkylation of glycal-derived π-allyl Pd(II) intermediates, prepared by oxidative addition of Pd(0) species to 2,3-unsaturated py

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