Cas 596119-91-4,Carbamic acid, [2-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-1-methyl-2-oxoethyl]methyl-, phenylmethyl ester

596119-91-4

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Basic information

Product Name: Carbamic acid, [2-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-1-methyl-2-oxoethyl]methyl-, phenylmethyl ester
Synonyms:
CAS NO:596119-91-4
Molecular Formula: C22H28N2O5
Molecular Weight: 400.475
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: Carbamic acid, [2-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-1-methyl-2-oxoethyl]methyl-, phenylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [2-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-1-methyl-2-oxoethyl]methyl-, phenylmethyl ester(596119-91-4)
EPA Substance Registry System: Carbamic acid, [2-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-1-methyl-2-oxoethyl]methyl-, phenylmethyl ester(596119-91-4)

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: 596119-91-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 596119-91-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,6,1,1 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 596119-91:
(8*5)+(7*9)+(6*6)+(5*1)+(4*1)+(3*9)+(2*9)+(1*1)=194
194 % 10 = 4
So 596119-91-4 is a valid CAS Registry Number.

596119-91-4Upstream product

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596119-91-4Relevant academic research and scientific papers

Synthesis and crystal structure of hydrogenated pyrazino [2,1-a]isoquinoline derivatives

Zawadzka,Leniewski,Maurin,Wojtasiewicz,Siwicka,Czarnocki

, p. 565 - 576 (2007/10/03)

Racemic amino acids (Ala and Val) were used in order to optimize the procedures and to check the stereochemical outcome of the synthesis of tetrahydroisoquinoline derivatives. The key step introduced the Pictet-Spengler condensation on ketoamides 4a and 4

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