Cas 270925-35-4,dimethyl (4S)-4-[N-((1R)-1-phenylethyl)-2,2,2-trifluoroacetylamino]-2-methylenepentane-1,5-dioate

270925-35-4

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Basic information

Product Name: dimethyl (4S)-4-[N-((1R)-1-phenylethyl)-2,2,2-trifluoroacetylamino]-2-methylenepentane-1,5-dioate
Synonyms: dimethyl (4S)-4-[N-((1R)-1-phenylethyl)-2,2,2-trifluoroacetylamino]-2-methylenepentane-1,5-dioate
CAS NO:270925-35-4
Molecular Formula:
Molecular Weight: 387.356
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: dimethyl (4S)-4-[N-((1R)-1-phenylethyl)-2,2,2-trifluoroacetylamino]-2-methylenepentane-1,5-dioate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl (4S)-4-[N-((1R)-1-phenylethyl)-2,2,2-trifluoroacetylamino]-2-methylenepentane-1,5-dioate(270925-35-4)
EPA Substance Registry System: dimethyl (4S)-4-[N-((1R)-1-phenylethyl)-2,2,2-trifluoroacetylamino]-2-methylenepentane-1,5-dioate(270925-35-4)

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: 270925-35-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 270925-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,0,9,2 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 270925-35:
(8*2)+(7*7)+(6*0)+(5*9)+(4*2)+(3*5)+(2*3)+(1*5)=144
144 % 10 = 4
So 270925-35-4 is a valid CAS Registry Number.

270925-35-4Upstream product

407-25-0 trifluoroacetic anhydride

270925-35-4Downstream Products

270925-36-5 dimethyl (2S)-2-[N-((1R)-1-phenylethyl)-2,2,2-trifluoroacetylamino]-4-oxopentane-1,5-dioate

270925-35-4Relevant academic research and scientific papers

Aldol reaction under solvent-free conditions: Highly stereoselective synthesis of 1,3-amino alcohols

Loh, Teck-Peng,Huang, Jing-Mei,Goh, Swee-Hock,Vittal, Jagadese J.

, p. 1291 - 1294 (2000)

(formula presented) A method for the highly stereoselective synthesis of 1,3-amino alcohols based on the indium trichloride-catalyzed Mukaiyama aldol reaction of keto ester (R,S)-1 under solvent-free conditions has been developed. The high selectivity obs

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