75795-07-2 Usage
Uses
Used in Plastics and Polymers Industry:
3,3',4,4'-Tetrachlorobenzophenone is used as a UV absorbent for [application reason] to protect plastics and polymers from degradation caused by exposure to ultraviolet radiation. This enhances the durability and longevity of the materials, making them more resistant to environmental factors.
Used in Dye and Pigment Production:
In the dye and pigment industry, 3,3',4,4'-Tetrachlorobenzophenone is used as an intermediate chemical for [application reason] the synthesis of various dyes and pigments. Its unique chemical structure contributes to the color properties and stability of the final products.
Used in Organic Compounds Synthesis:
3,3',4,4'-Tetrachlorobenzophenone is utilized as a key intermediate in the synthesis of other organic compounds for [application reason] its versatile chemical properties, allowing for the creation of a wide range of products with diverse applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 75795-07-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,9 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75795-07:
(7*7)+(6*5)+(5*7)+(4*9)+(3*5)+(2*0)+(1*7)=172
172 % 10 = 2
So 75795-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H6Cl4O/c14-9-3-1-7(5-11(9)16)13(18)8-2-4-10(15)12(17)6-8/h1-6H
75795-07-2Relevant academic research and scientific papers
Phosphate compounds and their use as medicaments
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, (2008/06/13)
A compound of the formula (I) or salts thereof: wherein X, R1, Q1 and Q2 are as defined in the specification. The compounds have been found to be P2 7-TM G-protein receptor antagonists, especially to the P2 Y2 receptor, and are useful in therapy, for example as anti-inflammatory agents useful in the treatment of a number of inflammatory diseases such as asthma, inflammatory bowel disease, ARDS, psoriasis, rheumatoid arthritis, myocardial ischaemia, COPD, cystic fibrosis, arthrosclerosis, restenosis, peridontal disease, septic shock, osteoarthritis and stroke
Method of making halobenzophenones and intermediates thereof
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, (2008/06/13)
Disclosed is a method of making a bisphenyl dihalomethane by reacting a trihalomethylbenzene with a halobenzene and a Lewis acid. The bisphenyl dihalomethane can than be reacted with water to form a halobenzophenone. In an optical third step ring chlorines that are present can be replaced with fluorines and, in a final step, any remaining chlorines can be removed to leave a fluorobenzophenone. The process is particularly useful in making 4,4'-difluorobenzophenone, which is in turn useful in making polyetheretherketones.
