Cas 220892-30-8,Methyl (S)-2,2-dimethyl-3-(2,4,6-trimethylphenyl)-3-[N-phenyl-((S)-N',N'-phthaloyl-tert-leucyl)]aminopropionate

220892-30-8

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Basic information

Product Name: Methyl (S)-2,2-dimethyl-3-(2,4,6-trimethylphenyl)-3-[N-phenyl-((S)-N',N'-phthaloyl-tert-leucyl)]aminopropionate
Synonyms: Methyl (S)-2,2-dimethyl-3-(2,4,6-trimethylphenyl)-3-[N-phenyl-((S)-N',N'-phthaloyl-tert-leucyl)]aminopropionate
CAS NO:220892-30-8
Molecular Formula:
Molecular Weight: 568.713
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)-2,2-dimethyl-3-(2,4,6-trimethylphenyl)-3-[N-phenyl-((S)-N',N'-phthaloyl-tert-leucyl)]aminopropionate(CAS DataBase Reference)
NIST Chemistry Reference: Methyl (S)-2,2-dimethyl-3-(2,4,6-trimethylphenyl)-3-[N-phenyl-((S)-N',N'-phthaloyl-tert-leucyl)]aminopropionate(220892-30-8)
EPA Substance Registry System: Methyl (S)-2,2-dimethyl-3-(2,4,6-trimethylphenyl)-3-[N-phenyl-((S)-N',N'-phthaloyl-tert-leucyl)]aminopropionate(220892-30-8)

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: 220892-30-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 220892-30-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,8,9 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 220892-30:
(8*2)+(7*2)+(6*0)+(5*8)+(4*9)+(3*2)+(2*3)+(1*0)=118
118 % 10 = 8
So 220892-30-8 is a valid CAS Registry Number.

220892-30-8Upstream product

220892-30-8Downstream Products

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

220892-30-8Relevant 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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