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5-(4-(trifluoromethyl)phenyl)hex-5-enoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1261280-20-9

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1261280-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1261280-20-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,2,8 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1261280-20:
(9*1)+(8*2)+(7*6)+(6*1)+(5*2)+(4*8)+(3*0)+(2*2)+(1*0)=119
119 % 10 = 9
So 1261280-20-9 is a valid CAS Registry Number.

1261280-20-9Relevant academic research and scientific papers

Enantioselective Organocatalyzed Bromolactonizations: Applications in Natural Product Synthesis

Aursnes, Marius,Tungen, J?rn E.,Hansen, Trond V.

, p. 8287 - 8295 (2016/09/28)

Asymmetric bromolactonization reactions of δ-unsaturated carboxylic acids have been investigated in the presence of 10 chiral squaramide hydrogen-bonding organocatalysts. The best catalyst enabled the cyclization of several 5-arylhex-5-enoic acids into th

Enantioselective bromolactonization using an S-alkyl thiocarbamate catalyst

Jiang, Xiaojian,Tan, Chong Kiat,Zhou, Ling,Yeung, Ying-Yeung

supporting information; experimental part, p. 7771 - 7775 (2012/09/07)

The apple never falls far from the tree: S-alkyl thiocarbamate 1 (see scheme, NBP=N-bromophthalimide) was prepared in high yield through a synthetic sequence involving a Newman-Kwart rearrangement of the corresponding O-alkyl thiocarbamates. Compound 1 was used to catalyze bromolactonization, thus providing enantioenriched δ-lactones in excellent yield and enantioselectivity. Copyright

Asymmetric bromolactonization catalyzed by a C3-symmetric chiral trisimidazoline

Murai, Kenichi,Matsushita, Tomoyo,Nakamura, Akira,Fukushima, Shunsuke,Shimura, Masato,Fujioka, Hiromichi

supporting information; experimental part, p. 9174 - 9177 (2011/02/26)

A productive alliance: In an enantioselective organocatalytic bromolactonization of 5-substituted hex-5-enoic acids (see scheme), it appears that the formation of an ion pair through interaction of the trisimidazoline catalyst 1 with the substrate both cr

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