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"Benzenamine, 2,6-dichloro-3,5-difluoro-" is a chemical compound with the molecular formula C6H3Cl2F2N. It is an aromatic amine derivative, characterized by the presence of a benzene ring with two chlorine atoms at the 2nd and 6th positions, and two fluorine atoms at the 3rd and 5th positions. The amine group (-NH2) is attached to the benzene ring, which can participate in various chemical reactions, such as acylation, alkylation, and nitration. Benzenamine, 2,6-dichloro-3,5-difluoro- has potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity. However, it is important to note that the compound may have certain hazards, such as being harmful if inhaled or absorbed through the skin, and requires proper handling and disposal.

700-15-2

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700-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 700-15-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 700-15:
(5*7)+(4*0)+(3*0)+(2*1)+(1*5)=42
42 % 10 = 2
So 700-15-2 is a valid CAS Registry Number.

700-15-2Upstream product

700-15-2Downstream Products

700-15-2Relevant academic research and scientific papers

Process for producing 3,5-difluoraniline

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, (2008/06/13)

A process for producing 3,5-difluoroaniline, which comprises reacting a benzonitrile compound of the formula (I): STR1 wherein each of X1, X2 and X3 is hydrogen, chlorine, bromine or a cyano group, provided that at least one of X1 to X3 is a cyano group, with a mineral acid for hydrolysis and decarboxylation to obtain an aniline compound of the formula (II): STR2 wherein each of X4, X5 and X6 is hydrogen, chlorine or bromine, provided that at least one of X4 to X6 is hydrogen, and in the case of a compound of the formula (II) wherein X4, X5 and X6 are not simultaneously hydrogen, reacting such a compound with hydrogen in a presence of a catalyst for reduction to obtain 3,5 -difluoroaniline.

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