145572-10-7 Usage
Uses
Used in Pharmaceutical Industry:
4-CHLORO-2,3,5,6-TETRAFLUOROBENZOYL CHLORIDE is used as an intermediate in the synthesis of various drugs. Its unique chemical structure allows for the development of new pharmaceutical compounds with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 4-CHLORO-2,3,5,6-TETRAFLUOROBENZOYL CHLORIDE serves as a key intermediate in the production of insecticides and other pesticides. Its reactivity enables the creation of effective compounds for pest control in agriculture.
Used in Dye and Pigment Manufacturing:
4-CHLORO-2,3,5,6-TETRAFLUOROBENZOYL CHLORIDE is utilized as a starting material in the manufacturing of dyes and pigments. Its chemical properties contribute to the development of vibrant and stable colorants for various applications.
Used in Adhesive Production:
4-CHLORO-2,3,5,6-TETRAFLUOROBENZOYL CHLORIDE is also employed in the production of adhesives, where its reactive nature aids in the formation of strong bonds between different materials.
Due to the reactivity and potential health hazards associated with 4-CHLORO-2,3,5,6-TETRAFLUOROBENZOYL CHLORIDE, it is crucial to handle and store it with appropriate safety measures to ensure the well-being of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 145572-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,5,7 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 145572-10:
(8*1)+(7*4)+(6*5)+(5*5)+(4*7)+(3*2)+(2*1)+(1*0)=127
127 % 10 = 7
So 145572-10-7 is a valid CAS Registry Number.
InChI:InChI=1/C7Cl2F4O/c8-2-5(12)3(10)1(7(9)14)4(11)6(2)13
145572-10-7Relevant articles and documents
Selective hydrolysis of pentafluorobenzotrichloride
Shipilov,Kolpashchikova,Igumnov
, p. 975 - 978 (2007/10/03)
Selective hydrolysis of pentafluorobenzotrichloride has been studied in the presence of a catalytic amount of iron(III) chloride. The main products are pentafluorobenzoyl chloride, pentafluorobenzoyl fluoride, and 4-chlorotetrafluorobenzoyl chloride. The two latter products are formed by hydrolysis of dichlorofluoromethylpentafluorobenzene and 4- chlorotetrafluorobenzotrichloride which result from halogen exchange between the methyl group and aromatic ring in the initial pentafluorobenzotrichloride. A probable mechanism for halogen exchange is proposed.
Synthesis and reactions of 4-sulpho-2,3,5,6-tetrafluorobenzoic acid
Fielding, H. C.,Shirley, I. M.
, p. 15 - 31 (2007/10/02)
4-Sulpho-2,3,5,6-tetrafluorobenzoic acid (I) has been synthesised from pentafluorobenzoic acid via the oxidation of 4-mercapto-tetrafluorobenzoic acid.Reaction of I with DMF/SOCl2 gave 1,4-ClC6F4COCl (IIA) which was converted to 1,4-ClC6F4COF (IIB) by flu
