103807-49-4 Usage
Uses
Used in Paints and Coatings Industry:
Alpha-bromo-4-chloro-benzene acetic acid isopropyl ester is used as a solvent to enhance the flow and application properties of paints and coatings. Its strong solvent characteristics allow for even distribution of pigments and binders, resulting in a smooth and uniform finish.
Used in Adhesives Production:
In the adhesives industry, this ester is employed as a solvent to improve the adhesive's bonding strength and flexibility. Its ability to dissolve various components ensures a consistent and effective adhesive formulation.
Used in Plastics Manufacturing:
Alpha-bromo-4-chloro-benzene acetic acid isopropyl ester is used as a processing aid in the production of plastics. It helps to lower the viscosity of the plastic melt, facilitating easier processing and molding.
Used in Textile Industry:
In the textile industry, this chemical is utilized as a solvent in dyeing and finishing processes. Its strong solvent properties enable even dye distribution and improved colorfastness of textiles.
Used in Personal Care Products:
Alpha-bromo-4-chloro-benzene acetic acid isopropyl ester is used in the formulation of personal care products, such as fragrances and cosmetics, to dissolve essential oils and other ingredients, ensuring a uniform and stable product.
Used as an Intermediate in Pharmaceutical and Agrochemical Synthesis:
This ester serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new and effective treatments and crop protection agents.
Check Digit Verification of cas no
The CAS Registry Mumber 103807-49-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,8,0 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103807-49:
(8*1)+(7*0)+(6*3)+(5*8)+(4*0)+(3*7)+(2*4)+(1*9)=104
104 % 10 = 4
So 103807-49-4 is a valid CAS Registry Number.
103807-49-4Relevant academic research and scientific papers
Utilization of natural sunlight and air in the aerobic oxidation of benzyl halides
Su, Yijin,Zhang, Liangren,Jiao, Ning
supporting information; body text, p. 2168 - 2171 (2011/06/21)
Chemical equations presented. A novel, efficient oxidation of α-aryl halogen derivatives to the corresponding α-aryl carbonyl compounds at room temperature has been disclosed. Natural sunlight and air are successfully utilized in this approach through the combination of photocatalysis and organocatalysis. A plausible mechanism was proposed on the basis of the mechanistic studies.
RESOLUTION OF α-(PHENOXY)PHENYLACETIC ACID DERIVATIVES
-
Page/Page column 35; 40 -41, (2010/02/10)
The present invention provides a method for producing an enantiomerically enriched alpha-(phenoxy)phenylacetic acid compound of the formula (I): from its enantiomeric mixture, where R1 is alkyl or haloalkyl and X is halide.
SYNTHESES D'ESTERS OU D'ACIDES α-HALOGENES A PARTIR DES GEM DICYANO EPOXIDES.
Robert, A.,Jaguelin, S.,Guinamant, J. L.
, p. 2275 - 2282 (2007/10/02)
α-halogeno esters or α-halogenoacids were easily prepared by selective one pot reaction of gem-dicyano epoxides with halohydric acids in an alcoholic or aqueous media.
