75024-22-5 Usage
General Description
1,4-Dibromo-2,3-dimethylbenzene, also known as 1,4-dibromo-2,3-xylene, is a chemical compound with the molecular formula C8H8Br2. It is a member of the class of compounds known as xylenes, which are aromatic hydrocarbons containing a benzene ring with two methyl groups and two bromine atoms attached to it. This chemical is a colorless to light yellow liquid with a strong odor, and it is mainly used as an intermediate in the production of various industrial and agricultural chemicals. It is also used in the manufacture of dyes, perfumes, and pharmaceuticals. 1,4-Dibromo-2,3-dimethylbenzene is considered to be toxic and may cause irritation to the skin, eyes, and respiratory system upon exposure.
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 articles and documents
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
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
