Cas 357615-94-2,5-Oxazolidinecarboxylic acid, 3-benzoyl-2-(2,4-dimethoxyphenyl)-4-(2-furanyl)-5-methyl-, methyl ester, (4S,5R)-

357615-94-2

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Basic information

Product Name: 5-Oxazolidinecarboxylic acid, 3-benzoyl-2-(2,4-dimethoxyphenyl)-4-(2-furanyl)-5-methyl-, methyl ester, (4S,5R)-
Synonyms:
CAS NO:357615-94-2
Molecular Formula: C25H25NO7
Molecular Weight: 451.476
EINECS: N/A
Product Categories: N/A
Mol File: 357615-94-2.mol

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: 5-Oxazolidinecarboxylic acid, 3-benzoyl-2-(2,4-dimethoxyphenyl)-4-(2-furanyl)-5-methyl-, methyl ester, (4S,5R)-(CAS DataBase Reference)
NIST Chemistry Reference: 5-Oxazolidinecarboxylic acid, 3-benzoyl-2-(2,4-dimethoxyphenyl)-4-(2-furanyl)-5-methyl-, methyl ester, (4S,5R)-(357615-94-2)
EPA Substance Registry System: 5-Oxazolidinecarboxylic acid, 3-benzoyl-2-(2,4-dimethoxyphenyl)-4-(2-furanyl)-5-methyl-, methyl ester, (4S,5R)-(357615-94-2)

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: 357615-94-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 357615-94-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,6,1 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 357615-94:
(8*3)+(7*5)+(6*7)+(5*6)+(4*1)+(3*5)+(2*9)+(1*4)=172
172 % 10 = 2
So 357615-94-2 is a valid CAS Registry Number.

357615-94-2Upstream product

98-88-4 benzoyl chloride

357615-94-2Downstream Products

630127-47-8 (4S,5R)-3-Benzoyl-2-(2,4-dimethoxy-phenyl)-4-furan-2-yl-5-methyl-oxazolidine-5-carboxylic acid

357615-94-2Relevant academic research and scientific papers

1′-Azido- and 1′-amino-1,3-dioxolan-4-ones

Battaglia, Arturo,Barbaro, Gaetano,Giorgianni, Patrizia,Guerrini, Andrea,Pepe, Antonella

, p. 1015 - 1023 (2007/10/03)

1,3-Dioxolanone alcohols, prepared via the addition of chiral lithium enolates of 1,3-dioxolan-4-ones to aldehydes, are suitable intermediates for the synthesis of chiral trisubstituted isoserines or trisubstituted 3-hydroxy-β-lactams. In particular, the

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