Cas 254763-20-7,2-Pentenoic acid, 4-[(chlorophenylacetyl)amino]-5-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-, ethyl ester, (2E)-

254763-20-7

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Basic information

Product Name: 2-Pentenoic acid, 4-[(chlorophenylacetyl)amino]-5-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-, ethyl ester, (2E)-
Synonyms:
CAS NO:254763-20-7
Molecular Formula: C31H36ClNO4Si
Molecular Weight: 550.17
EINECS: N/A
Product Categories: N/A
Mol File: 254763-20-7.mol

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: 2-Pentenoic acid, 4-[(chlorophenylacetyl)amino]-5-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-, ethyl ester, (2E)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Pentenoic acid, 4-[(chlorophenylacetyl)amino]-5-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-, ethyl ester, (2E)-(254763-20-7)
EPA Substance Registry System: 2-Pentenoic acid, 4-[(chlorophenylacetyl)amino]-5-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-, ethyl ester, (2E)-(254763-20-7)

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: 254763-20-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 254763-20-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,4,7,6 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 254763-20:
(8*2)+(7*5)+(6*4)+(5*7)+(4*6)+(3*3)+(2*2)+(1*0)=147
147 % 10 = 7
So 254763-20-7 is a valid CAS Registry Number.

254763-20-7Upstream product

2912-62-1 α-chlorophenylacetyl chloride

254763-20-7Downstream Products

254763-20-7Relevant academic research and scientific papers

Efficient tin hydride-mediated radical cyclisation of secondary amides leading to substituted pyrrolidinones. Part 2. Application to the synthesis of aromatic kainic acid analogues

Bryans, Justin S.,Large, Jonathan M.,Parsons, Andrew F.

, p. 2905 - 2910 (1999)

An enantioselective synthesis of phenyl allokainoid, starting from D-serine, is reported. Tin-mediated cyclisation of a secondary amide was used in the key step to produce a trisubstituted pyrrolidinone in excellent yield (ca. 80%). The predominant format

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