Cas 143439-64-9,Carbamic acid, [2-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-2-oxo-1-(phenylmethyl)ethyl]-, phenylmethyl ester, (S)-

143439-64-9

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Basic information

Product Name: Carbamic acid, [2-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-2-oxo-1-(phenylmethyl)ethyl]-, phenylmethyl ester, (S)-
Synonyms:
CAS NO:143439-64-9
Molecular Formula: C27H30N2O5
Molecular Weight: 462.546
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]-2-oxo-1-(phenylmethyl)ethyl]-, phenylmethyl ester, (S)-(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [2-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-2-oxo-1-(phenylmethyl)ethyl]-, phenylmethyl ester, (S)-(143439-64-9)
EPA Substance Registry System: Carbamic acid, [2-[[2-(3,4-dimethoxyphenyl)ethyl]amino]-2-oxo-1-(phenylmethyl)ethyl]-, phenylmethyl ester, (S)-(143439-64-9)

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: 143439-64-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 143439-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,4,3 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 143439-64:
(8*1)+(7*4)+(6*3)+(5*4)+(4*3)+(3*9)+(2*6)+(1*4)=129
129 % 10 = 9
So 143439-64-9 is a valid CAS Registry Number.

143439-64-9Upstream product

143439-64-9Downstream Products

603121-72-8 (2S)-2-amino-N-[2-(3,4-dimethoxyphenyl)ethyl]-3-phenylpropanamide

143439-64-9Relevant academic research and scientific papers

Diastereoselective synthesis of 1-benzyltetrahydroisoquinoline derivatives from amino acids by 1,4 chirality transfer

Zawadzka, Anna,Leniewski, Andrzej,Maurin, Jan K.,Wojtasiewicz, Krystyna,Siwicka, Aleksandra,Blachut, Dariusz,Czarnocki, Zbigniew

, p. 2443 - 2453 (2007/10/03)

L-Amino acids (L-Ala, L-Phe, L-Val, L-Pro) were used as a source of chirality in the diastereoselective synthesis of tetrahydroisoquinoline derivatives. The key step was the Pictet-Spengler condensation of ketoamides 4 and 10, which proceeded under very m

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