75024-22-5 Usage
Uses
Used in Chemical Synthesis:
1,4-Dibromo-2,3-dimethylbenzene is used as an intermediate in the chemical synthesis industry for the production of a variety of industrial and agricultural chemicals. Its unique structure allows for versatile reactions and transformations, making it a valuable component in the synthesis of target compounds.
Used in Dye Manufacturing:
In the dye industry, 1,4-dibromo-2,3-xylene is employed as a key intermediate for the production of various dyes. Its bromine atoms facilitate the formation of color-producing chromophores, contributing to the development of a wide range of dyes with different color characteristics.
Used in Perfumery:
1,4-Dibromo-2,3-dimethylbenzene is utilized in the perfume industry as a precursor for the synthesis of fragrance compounds. Its aromatic nature and bromine-containing structure enable the creation of unique scent profiles, enhancing the variety of perfumes available in the market.
Used in Pharmaceutical Production:
In the pharmaceutical sector, 1,4-dibromo-2,3-xylene serves as a crucial intermediate for the synthesis of various medicinal compounds. Its chemical properties allow for the development of drugs with specific therapeutic effects, contributing to the advancement of healthcare and medicine.
Used in Pesticide Formulation:
1,4-Dibromo-2,3-dimethylbenzene is also employed in the agricultural industry for the formulation of pesticides. Its chemical properties enable the development of effective pest control agents, helping to protect crops and ensure food security.
Check Digit Verification of cas no
The CAS Registry Mumber 75024-22-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,2 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75024-22:
(7*7)+(6*5)+(5*0)+(4*2)+(3*4)+(2*2)+(1*2)=105
105 % 10 = 5
So 75024-22-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H8Br2/c1-5-6(2)8(10)4-3-7(5)9/h3-4H,1-2H3
75024-22-5Relevant academic research and scientific papers
Amplifying fluorescent conjugated polymer sensor for singlet oxygen detection
Wang, Chun-Han,Nesterov, Evgueni E.
supporting information, p. 8955 - 8958 (2019/07/31)
A "higher energy gap" concept was applied towards designing an efficient turn-on amplifying sensor for singlet oxygen-an important biomedical and environmental monitoring analytical target. The concept is based on modulation of intramolecular energy trans
A novel amino-benzosuberone derivative is a picomolar inhibitor of mammalian aminopeptidase N/CD13
Maiereanu, Carmen,Schmitt, Céline,Schifano-Faux, Nadge,Le Nou?n, Didier,Defoin, Albert,Tarnus, Céline
experimental part, p. 5716 - 5733 (2011/10/12)
A new class of low molecular weight, highly potent and selective non peptidic inhibitors of aminopeptidase N (APN/CD13) is described. We report the synthesis and in vitro evaluation of racemic substituted analogues of 7-amino-benzocyclohepten-6-one 1a. We
Synthesis and Rigid Conformers of 14,15-Dimethyl-2,11-dithia(1,3)(1,4)cyclophane and 12,13-Dimethyl(1,3)(1,4)cyclophane
Lai, Yee-Hing,Yap, Angeline Hui-Tin
, p. 1373 - 1377 (2007/10/02)
The dithiacyclophane 4 was synthesized from 2,3-dimethylaniline in seven steps.Only the conformer 5b was isolated.Photodesulfurization of 4b however resulted only in the isolation of the cyclophane 2a indicating an abrupt change in conformational preferen
