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4-Pentynoic acid, 2-[(phenylsulfonyl)amino]-2-(trifluoromethyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

929616-37-5

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929616-37-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 929616-37-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,6,1 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 929616-37:
(8*9)+(7*2)+(6*9)+(5*6)+(4*1)+(3*6)+(2*3)+(1*7)=205
205 % 10 = 5
So 929616-37-5 is a valid CAS Registry Number.

929616-37-5Downstream Products

929616-37-5Relevant academic research and scientific papers

Synthesis of α-Alkynyl-β,β,β-trifluoroalanine Derivatives by Sonogashira Cross-Coupling Reaction

Shchetnikov, Grigorii T.,Zotova, Maria A.,Bruneau, Christian,Dixneuf, Pierre H.,Osipov, Sergey N.

experimental part, p. 1587 - 1592 (2010/06/15)

An efficient route to new a-CF3-a-amino acid derivatives bearing an arylalkynyl moiety at the a-carbon atom has been developed. The method is based on palladium-catalyzed cross-coupling of the corresponding a-propargyl (ethynyl) a- amino esters

Ruthenium-catalyzed cyclotrimerization of 1,6- and 1,7-azadiynes: New access to fluorinated bicyclic amino acids

Shchetnikov, Grigorii T.,Osipov, Sergey N.,Bruneau, Christian,Dixneuf, Pierre H.

, p. 578 - 582 (2008/12/22)

An efficient access to a variety of trifluoromethyl-substituted cyclic α-amino acid derivatives based on ruthenium-catalyzed cyclotrimerization of appropriate 1,6- and 1,7-diynes with terminal and internal alkynes has been developed. Georg Thieme Verlag S

Effective pathway to the α-CF3-substituted azahistidine analogues

Shchetnikov, Grigorii T.,Peregudov, Alexander S.,Osipov, Sergej N.

, p. 136 - 140 (2008/03/13)

An efficient method for the preparation of functionalized α-trifluoromethyl-substituted azahistidine analogues has been developed. The method is based on the regioselective addition of allenylmagnesiumbromide to highly electrophilic imines of trifluoropyr

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