Cas 440370-34-3,4-[(2-hydroxy-1-methyl-2-phenylethyl)-methylcarbamoyl]-3-(4-methoxyphenoxymethyl)-4-phenylbutyric acid methyl ester

440370-34-3

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Basic information

Product Name: 4-[(2-hydroxy-1-methyl-2-phenylethyl)-methylcarbamoyl]-3-(4-methoxyphenoxymethyl)-4-phenylbutyric acid methyl ester
Synonyms: 4-[(2-hydroxy-1-methyl-2-phenylethyl)-methylcarbamoyl]-3-(4-methoxyphenoxymethyl)-4-phenylbutyric acid methyl ester
CAS NO:440370-34-3
Molecular Formula:
Molecular Weight: 505.611
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-[(2-hydroxy-1-methyl-2-phenylethyl)-methylcarbamoyl]-3-(4-methoxyphenoxymethyl)-4-phenylbutyric acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-[(2-hydroxy-1-methyl-2-phenylethyl)-methylcarbamoyl]-3-(4-methoxyphenoxymethyl)-4-phenylbutyric acid methyl ester(440370-34-3)
EPA Substance Registry System: 4-[(2-hydroxy-1-methyl-2-phenylethyl)-methylcarbamoyl]-3-(4-methoxyphenoxymethyl)-4-phenylbutyric acid methyl ester(440370-34-3)

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: 440370-34-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 440370-34-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,0,3,7 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 440370-34:
(8*4)+(7*4)+(6*0)+(5*3)+(4*7)+(3*0)+(2*3)+(1*4)=113
113 % 10 = 3
So 440370-34-3 is a valid CAS Registry Number.

440370-34-3Upstream product

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440370-34-3Relevant academic research and scientific papers

Michael Reactions of Pseudoephedrine Amide Enolates: Effect of LiCl on Syn/Anti Selectivity

Smitrovich, Jacqueline H.,DiMichele, Lisa,Qu, Chuanxing,Boice, Genevieve N.,Nelson, Todd D.,Huffman, Mark A.,Murry, Jerry

, p. 1903 - 1908 (2007/10/03)

The stereochemical outcome of the asymmetric Michael reaction of pseudoephedrine amide enolates changes dramatically in the presence of LiCl. Reaction of the enolate in the absence of LiCl results in formation of the anti Michael adduct with high selectiv

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