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(S)-1-cyclohexyl-4-methyl-pent-2-yne-1,4-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

321855-40-7

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321855-40-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 321855-40-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,8,5 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 321855-40:
(8*3)+(7*2)+(6*1)+(5*8)+(4*5)+(3*5)+(2*4)+(1*0)=127
127 % 10 = 7
So 321855-40-7 is a valid CAS Registry Number.

321855-40-7Relevant academic research and scientific papers

Palladium-catalyzed construction of polycyclic heterocycles by an alkyne insertion and direct arylation cascade

Ohno, Hiroaki,Yamamoto, Mio,Iuchi, Mutsumi,Fujii, Nobutaka,Tanaka, Tetsuaki

scheme or table, p. 2567 - 2578 (2011/10/04)

Cascade cyclization of bromoenynes bearing an aryl group with catalytic amounts of palladium(II) acetate and cesium carbonate led to the direct construction of tri- or tetracyclic heterocycles. Direct arylation of a pyrrole, furan or thiophene ring in the

Ligand accelerated indium(III)-catalyzed asymmetric alkynylation of aldehydes with 2-methyl-3-butyn-2-ol as an ethyne equivalent donor

Harada, Shinji,Takita, Ryo,Ohshima, Takashi,Matsunaga, Shigeki,Shibasaki, Masakatsu

, p. 948 - 950 (2008/01/06)

Indium(III)-catalyzed asymmetric alkynylation of aryl, heteroaryl, alkyl and alkenyl aldehydes with 2-methyl-3-butyn-2-ol as an ethyne equivalent donor was realized, and products were obtained in moderate to good yields (up to 97%) and high enantioselecti

Enantioselective addition of 2-methyl-3-butyn-2-ol to aldehydes: Preparation of 3-hydroxy-1-butynes

Boyall,López,Sasaki,Frantz,Carreira

, p. 4233 - 4236 (2007/10/03)

(equation presented) We report the first example of enantioselective aldehyde additions of 2-methyl-3-butyn-2-ol, a commodity bulk chemical that is readily available. Following a facile fragmentation reaction, the addition reactions provide access to opti

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