Cas 152976-10-8,(E)-(S)-4-[Benzyl-(2,2,2-trichloro-acetyl)-amino]-5-(tert-butyl-dimethyl-silanyloxy)-pent-2-enoic acid ethyl ester

152976-10-8

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Basic information

Product Name: (E)-(S)-4-[Benzyl-(2,2,2-trichloro-acetyl)-amino]-5-(tert-butyl-dimethyl-silanyloxy)-pent-2-enoic acid ethyl ester
Synonyms: (E)-(S)-4-[Benzyl-(2,2,2-trichloro-acetyl)-amino]-5-(tert-butyl-dimethyl-silanyloxy)-pent-2-enoic acid ethyl ester
CAS NO:152976-10-8
Molecular Formula:
Molecular Weight: 508.945
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: (E)-(S)-4-[Benzyl-(2,2,2-trichloro-acetyl)-amino]-5-(tert-butyl-dimethyl-silanyloxy)-pent-2-enoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(S)-4-[Benzyl-(2,2,2-trichloro-acetyl)-amino]-5-(tert-butyl-dimethyl-silanyloxy)-pent-2-enoic acid ethyl ester(152976-10-8)
EPA Substance Registry System: (E)-(S)-4-[Benzyl-(2,2,2-trichloro-acetyl)-amino]-5-(tert-butyl-dimethyl-silanyloxy)-pent-2-enoic acid ethyl ester(152976-10-8)

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: 152976-10-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 152976-10-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,9,7 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 152976-10:
(8*1)+(7*5)+(6*2)+(5*9)+(4*7)+(3*6)+(2*1)+(1*0)=148
148 % 10 = 8
So 152976-10-8 is a valid CAS Registry Number.

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152976-10-8Relevant academic research and scientific papers

A Highly Efficient Free Radical Approach to Trisubstituted Pyrrolidinones

Parsons, A. F.,Taylor, R. J. K.

, p. 1224 - 1225 (1993)

The radical-mediated cyclisation of serine derived α-chloroamides has been found to be influenced in both yield and stereoselectivity by the nature of the substituent at the site of radical generation-radicals substituted at the α-position by methyl, phen

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