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1-Propyn-1-amine,3,3,3-trifluoro-N,N-dimethyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

211803-07-5

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211803-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 211803-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,8,0 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 211803-07:
(8*2)+(7*1)+(6*1)+(5*8)+(4*0)+(3*3)+(2*0)+(1*7)=85
85 % 10 = 5
So 211803-07-5 is a valid CAS Registry Number.

211803-07-5Relevant academic research and scientific papers

A new practical and convenient access to the synthesis of N,N-dialkyl-3,3,3-trifluoropropanamides

Yamanaka, Hiroki,Mantani, Toshiya,Shiomi, Keisuke,Ishihara, Takashi

, p. 615 - 616 (1998)

N,N-Dialkyl-3,3,3-trifluoropropanamides were readily synthesized in good to excellent yields through N,N-dialkyl(3,3,3-trifluoro-1-propynyl)amines, which were generated by the reaction of N,N-dialkyl(2,2,3,3,3-pentafluoropropyl)-or -(2,3,3,3-tetrafluoro-1

Preparation of trifluoromethylated ynamines and their reactions with some electrophilic reagents

Ishihara, Takashi,Mantani, Toshiya,Konno, Tsutomu,Yamanaka, Hiroki

, p. 3783 - 3793 (2007/10/03)

N,N-Dialkyl(3,3,3-trifluoro-1-propynyl)amines were prepared by a three-step procedure starting from commercially available 2,2,3,3,3-pentafluoropropanol. The reactions of these trifluoromethylated ynamines with some electrophiles, such as aldehydes, halog

A convenient preparation of 3,3,3-trifluoro-1-propynylamines and their Lewis acid catalyzed reaction with carbonyl compounds leading to (Z)-α-(trifluoromethyl)-α,β-unsaturated amides

Mantani,Shiomi,Konno,Ishihara,Yamanaka

, p. 3442 - 3448 (2007/10/03)

N,N-Dialkyl(3,3,3-trifluoro-1-propynyl)amines were readily prepared by a three-step procedure starting from commercially available 2,2,3,3,3-pentafluoropropanol. These fluorinated alkynylamines reacted smoothly with a variety of aldehydes or ketones in the presence of a catalytic amount of Lewis acid and molecular sieves 4A at ambient temperature to produce the corresponding α(trifluoromethyl)-α,β-unsaturated amides in good to excellent yields with high Z-stereoselectivity.

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