Cas 1027294-96-7,3-phenyl-2-((phenylacetyl)(trimethylsilanylmethyl)amino)propionic acid methyl ester

1027294-96-7

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Basic information

Product Name: 3-phenyl-2-((phenylacetyl)(trimethylsilanylmethyl)amino)propionic acid methyl ester
Synonyms: 3-phenyl-2-((phenylacetyl)(trimethylsilanylmethyl)amino)propionic acid methyl ester
CAS NO:1027294-96-7
Molecular Formula:
Molecular Weight: 383.563
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: 3-phenyl-2-((phenylacetyl)(trimethylsilanylmethyl)amino)propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-phenyl-2-((phenylacetyl)(trimethylsilanylmethyl)amino)propionic acid methyl ester(1027294-96-7)
EPA Substance Registry System: 3-phenyl-2-((phenylacetyl)(trimethylsilanylmethyl)amino)propionic acid methyl ester(1027294-96-7)

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: 1027294-96-7(Hazardous Substances Data)

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1027294-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1027294-96-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,2,9 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1027294-96:
(9*1)+(8*0)+(7*2)+(6*7)+(5*2)+(4*9)+(3*4)+(2*9)+(1*6)=147
147 % 10 = 7
So 1027294-96-7 is a valid CAS Registry Number.

1027294-96-7Upstream product

1027294-96-7Downstream Products

1027294-99-0 2-((methoxymethyl)(phenylacetyl)amino)-3-phenylpropionic acid methyl ester

1027294-96-7Relevant academic research and scientific papers

Building addressable libraries: Site-selective formation of an N-acyliminium ion intermediate

Kesselring, David,Maurer, Karl,Moeller, Kevin D.

, p. 2501 - 2504 (2008)

(Chemical Equation Presented) A strategy for site-selectively generating reactive N-acyliminium ion intermediates on a microelectrode array has been developed. The route capitalizes on the use of an electroauxiliary for building a methoxylated amino acid

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