Cas 313478-63-6,Methyl (S)-dimethyl-3-(2',4',6'-trimethylphenyl)-3-[N-phenyl-((S)-tert-leucyl)]aminopropionate

313478-63-6

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Basic information

Product Name: Methyl (S)-dimethyl-3-(2',4',6'-trimethylphenyl)-3-[N-phenyl-((S)-tert-leucyl)]aminopropionate
Synonyms: Methyl (S)-dimethyl-3-(2',4',6'-trimethylphenyl)-3-[N-phenyl-((S)-tert-leucyl)]aminopropionate
CAS NO:313478-63-6
Molecular Formula:
Molecular Weight: 438.61
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: Methyl (S)-dimethyl-3-(2',4',6'-trimethylphenyl)-3-[N-phenyl-((S)-tert-leucyl)]aminopropionate(CAS DataBase Reference)
NIST Chemistry Reference: Methyl (S)-dimethyl-3-(2',4',6'-trimethylphenyl)-3-[N-phenyl-((S)-tert-leucyl)]aminopropionate(313478-63-6)
EPA Substance Registry System: Methyl (S)-dimethyl-3-(2',4',6'-trimethylphenyl)-3-[N-phenyl-((S)-tert-leucyl)]aminopropionate(313478-63-6)

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: 313478-63-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 313478-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,4,7 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 313478-63:
(8*3)+(7*1)+(6*3)+(5*4)+(4*7)+(3*8)+(2*6)+(1*3)=136
136 % 10 = 6
So 313478-63-6 is a valid CAS Registry Number.

313478-63-6Upstream product

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313478-63-6Relevant academic research and scientific papers

Asymmetric steering of the Mannich reaction with phthaloyl amino acids

Mueller, Roland,Roettele, Herbert,Henke, Henning,Waldmann, Herbert

, p. 2032 - 2043 (2007/10/03)

Mannich-type reactions are powerful methods for the efficient synthesis of β-amino carbonyl compounds that are valuable intermediates for the construction of natural products, β-peptides, and peptidomimetics. For the efficient steric steering of Mannich r

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