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3-Fluoro-N-propylaniline is an organic chemical compound with the molecular formula C9H12FN. It is a derivative of aniline, featuring a fluorine atom at the 3-position and a propyl group attached to the nitrogen atom. 3-fluoro-N-propylaniline is a colorless liquid with a density of 1.01 g/cm3 and a boiling point of 220°C. It is soluble in common organic solvents such as ethanol, acetone, and dichloromethane. 3-Fluoro-N-propylaniline is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its potential applications in the chemical industry, it is essential to handle 3-fluoro-N-propylaniline with care, as it may have toxic effects and should be stored away from heat and open flames.

2806-11-3

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2806-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2806-11-3 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, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2806-11:
(6*2)+(5*8)+(4*0)+(3*6)+(2*1)+(1*1)=73
73 % 10 = 3
So 2806-11-3 is a valid CAS Registry Number.

2806-11-3Downstream Products

2806-11-3Relevant academic research and scientific papers

Titanium-Catalyzed Hydroaminoalkylation of Ethylene

Rosien, Michael,T?ben, Iris,Schmidtmann, Marc,Beckhaus, Rüdiger,Doye, Sven

supporting information, p. 2138 - 2142 (2020/02/05)

The first examples of titanium-catalyzed hydroaminoalkylation reactions of ethylene with secondary amines are presented. The reactions can be achieved with various titanium catalysts and they do not require the use of high pressure equipment. In addition, the first solid-state structure of a titanapyrrolidine that is formed by insertion of an alkene into the Ti?C bond of a titanaaziridine is reported.

Assembly of substituted 2-alkylquinolines by a sequential palladium-catalyzed Ci-N and Ci-C bond formation

Matsubara, Yoshio,Hirakawa, Saori,Yamaguchi, Yoshihiro,Yoshida, Zen-Ichi

experimental part, p. 7670 - 7673 (2011/10/05)

Diversity: A range of substituted 2-alkylquinolines can be prepared in a general and efficient synthetic approach that employs mild reaction conditions (see scheme). The synthesis is based on a sequential palladium-catalyzed Ci-N and Ci-C bond formation, followed by palladium-catalyzed aromatization, and results in the formation of the desired compounds in one step. Copyright

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