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2-Propynoic acid, 3-[2-(trifluoromethyl)phenyl]-, also known as 3-(2-trifluoromethylphenyl)prop-2-ynoic acid, is an organic compound characterized by its unique structure. It features a propynoic acid backbone with a triple bond between the first and second carbon atoms, and a phenyl ring substituted at the 2-position with a trifluoromethyl group. 2-Propynoic acid, 3-[2-(trifluoromethyl)phenyl]- is of interest in organic chemistry and material science due to its potential applications in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its molecular formula is C10H5F3O2, and it has a molecular weight of 216.14 g/mol. The presence of the trifluoromethyl group imparts specific electronic and steric properties to the molecule, which can influence its reactivity and physical characteristics.

2806-31-7

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2806-31-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2806-31-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2806-31:
(6*2)+(5*8)+(4*0)+(3*6)+(2*3)+(1*1)=77
77 % 10 = 7
So 2806-31-7 is a valid CAS Registry Number.

2806-31-7Relevant academic research and scientific papers

Structural design and synthesis of arylalkynyl amide-type peroxisome proliferator-activated receptor γ3 (PPAR γ3)-selective antagonists based on the helix12-folding inhibition hypothesis

Ohashi, Masao,Gamo, Kanae,Tanaka, Yuta,Waki, Minoru,Beniyama, Yoko,Matsuno, Kenji,Wada, Jun,Tenta, Masafumi,Eguchi, Jun,Makishima, Makoto,Matsuura, Nobuyasu,Oyama, Takuji,Miyachi, Hiroyuki

, p. 53 - 67 (2015/01/08)

Peroxisome proliferator-activated receptor γ3 (PPARγ3) antagonists are candidates for treatment of type 2 diabetes, obesity and osteoporosis. However, few rational design strategies are currently available. Here, we utilized the helix12 (H12)-folding inhi

Enantioselective synthesis of axially chiral phthalides through cationic [Rh1(H8-binap)]-catalyzed cross alkyne cyclotrimerization

Tanaka, Ken,Nishida, Goushi,Wada, Azusa,Noguchi, Keiichi

, p. 6510 - 6512 (2007/10/03)

(Chemical equation presented). Easy access to axially chiral phthalides that bear one or two oxymethylene functionalities is provided by an enantioselective cross alkyne cyclotrimerization in the presence of the cationic complex [Rh1{(S)-H8-binap}]+. The axial chirality is introduced during the formation of the benzene ring with high enantioselectivity.

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