Cas 143100-03-2,(1S,2R,4R)-10-dicyclohexylsulfamoylisobornyl (S)-3-phenyl-2-cyanopropanoate

143100-03-2

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Basic information

Product Name: (1S,2R,4R)-10-dicyclohexylsulfamoylisobornyl (S)-3-phenyl-2-cyanopropanoate
Synonyms:
CAS NO:143100-03-2
Molecular Formula:
Molecular Weight: 554.794
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: (1S,2R,4R)-10-dicyclohexylsulfamoylisobornyl (S)-3-phenyl-2-cyanopropanoate(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2R,4R)-10-dicyclohexylsulfamoylisobornyl (S)-3-phenyl-2-cyanopropanoate(143100-03-2)
EPA Substance Registry System: (1S,2R,4R)-10-dicyclohexylsulfamoylisobornyl (S)-3-phenyl-2-cyanopropanoate(143100-03-2)

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: 143100-03-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 143100-03-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,1,0 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 143100-03:
(8*1)+(7*4)+(6*3)+(5*1)+(4*0)+(3*0)+(2*0)+(1*3)=62
62 % 10 = 2
So 143100-03-2 is a valid CAS Registry Number.

143100-03-2Upstream product

132640-95-0 (1S,2R,4R)-10-dicyclohexylsulfamoylisobornyl (E)-2-cyanocinnamate

143100-03-2Downstream Products

143100-03-2Relevant academic research and scientific papers

Chiral 2-Cyanocinnamates in Conjugate Addition Asymmetric Enolate Trapping Reactions

Cativiela, Carlos,Diaz-de-Villegas, Maria Dolores,Galvez, Jose Antonio

, p. 1657 - 1661 (2007/10/02)

Chiral 2-cyannocinnamates react with L-selectride to give an intermediate enolate which can be stereoselectively trapped with different halides to afford α-substituted phenylalanine precursors with excellent chemical yields and good diastereomeric excess.

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