14845-75-1 Usage
Description
[1,1-Biphenyl]-2,2,6,6-tetrol,4,4-dimethyl-(9CI) is a complex and specific chemical compound that belongs to the category of polyphenols, which are compounds containing multiple phenol groups. It is known for its antioxidant properties and potential health benefits, making it a versatile and important compound in the chemical and pharmaceutical industries.
Uses
Used in Organic Chemistry Research:
[1,1-Biphenyl]-2,2,6,6-tetrol,4,4-dimethyl-(9CI) is used as a research compound for its unique structure and properties, contributing to the advancement of organic chemistry.
Used in Pharmaceutical Development:
In the pharmaceutical industry, [1,1-Biphenyl]-2,2,6,6-tetrol,4,4-dimethyl-(9CI) is used as a potential candidate for drug development due to its antioxidant properties and potential health benefits.
Used in Industrial Product Production:
[1,1-Biphenyl]-2,2,6,6-tetrol,4,4-dimethyl-(9CI) is also utilized as a raw material or intermediate in the production of various industrial products such as plastics, dyes, and other materials, enhancing their quality and performance.
Check Digit Verification of cas no
The CAS Registry Mumber 14845-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,4 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14845-75:
(7*1)+(6*4)+(5*8)+(4*4)+(3*5)+(2*7)+(1*5)=121
121 % 10 = 1
So 14845-75-1 is a valid CAS Registry Number.
14845-75-1Relevant articles and documents
Ba-catalyzed direct mannich-type reactions of a β,γ-unsaturated ester providing β-methyl aza-Morita - Baylis - Hillman-type products
Yamaguchi, Akitake,Aoyama, Naohiro,Matsunaga, Shigeki,Shibasaki, Masakatsu
, p. 3387 - 3390 (2007)
Barium-catalyzed direct Mannich-type reactions of a β,γ- unsaturated ester are described. The Ba-catalyst not only promoted the Mannich-type reactions, but also isomerized Mannich adducts to afford β-methyl aza-Morita - Baylis - Hillman-type products in 6
KINETICS OF OXIDATIVE COUPLING OF PHENOLS. OXIDATION OF RESORCINOLS BY ALKALINE HEXACYANOFERRATE (III)
Bhattacharjee, Mitra,Mahanti, Mahendra K.
, p. 1099 - 1105 (2007/10/02)
The reactions of resorcinol and 5-methylresorcinol (orcinol) with alkaline hexacyanoferrate(III), at constant ionic strength, gave coupled products.The rate of the reaction was dependent on the first power of concentration of each substrate, oxidant and alkali.The reaction pathway could be mechanistically visualized as proceeding via a radical intermediate formed in the rate determining step.This radical intermediate was detected by ESR spectroscopy, and showed an absorption in the visible region, and a typical absorption band at 1560 cm-1 in its infrared spectrum.
