Cas 879571-99-0,ethyl (2R)-4-(3,5-bis-trifluoromethyl-phenyl)-2-(2-methyl-prop-2-yl-(R)-sulfinylamino)-pent-4-enoate

879571-99-0

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Basic information

Product Name: ethyl (2R)-4-(3,5-bis-trifluoromethyl-phenyl)-2-(2-methyl-prop-2-yl-(R)-sulfinylamino)-pent-4-enoate
Synonyms: ethyl (2R)-4-(3,5-bis-trifluoromethyl-phenyl)-2-(2-methyl-prop-2-yl-(R)-sulfinylamino)-pent-4-enoate
CAS NO:879571-99-0
Molecular Formula:
Molecular Weight: 459.453
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: ethyl (2R)-4-(3,5-bis-trifluoromethyl-phenyl)-2-(2-methyl-prop-2-yl-(R)-sulfinylamino)-pent-4-enoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl (2R)-4-(3,5-bis-trifluoromethyl-phenyl)-2-(2-methyl-prop-2-yl-(R)-sulfinylamino)-pent-4-enoate(879571-99-0)
EPA Substance Registry System: ethyl (2R)-4-(3,5-bis-trifluoromethyl-phenyl)-2-(2-methyl-prop-2-yl-(R)-sulfinylamino)-pent-4-enoate(879571-99-0)

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: 879571-99-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 879571-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,5,7 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 879571-99:
(8*8)+(7*7)+(6*9)+(5*5)+(4*7)+(3*1)+(2*9)+(1*9)=250
250 % 10 = 0
So 879571-99-0 is a valid CAS Registry Number.

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879571-99-0Downstream Products

879571-99-0Relevant academic research and scientific papers

Enantioselective synthesis of non-proteinogenic 2-arylallyl-α-amino acids via Pd/In catalytic cascades

Grigg, Ronald,McCaffrey, Shaun,Sridharan, Visuvanathar,Fishwick, Colin W.G.,Kilner, Colin,Korn, Stewart,Bailey, Kevin,Blacker, John

, p. 12159 - 12171 (2007/10/03)

An efficient synthesis of both R- and S-enantiomers of 2-arylallyl-α-amino acids via a diastereoselective Pd/In mediated catalytic allylation of chiral N-sulfinyl-α-imino esters is described. The potential for further enhancement of molecular complexity a

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