43029-70-5 Usage
General Description
4-HYDROXY-4'-METHYL-BIPHENYL-3-CARBOXYLIC ACID is a chemical compound that belongs to the class of biphenyl carboxylic acids. It is a derivative of biphenyl, a type of aromatic hydrocarbon, with a hydroxyl group and a carboxylic acid group attached to the biphenyl core. 4-HYDROXY-4'-METHYL-BIPHENYL-3-CARBOXYLIC ACID is used in various industrial and research applications, including as a precursor for the synthesis of pharmaceuticals, agrochemicals, and materials. It is also a potential ligand for coordination chemistry and may have biological activity, making it a molecule of interest for medicinal and biological studies. Its structural and chemical properties make it an important compound in the field of organic chemistry and related disciplines.
Check Digit Verification of cas no
The CAS Registry Mumber 43029-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,0,2 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 43029-70:
(7*4)+(6*3)+(5*0)+(4*2)+(3*9)+(2*7)+(1*0)=95
95 % 10 = 5
So 43029-70-5 is a valid CAS Registry Number.
43029-70-5Relevant articles and documents
Green synthesis of biphenyl carboxylic acids via Suzuki–Miyaura cross-coupling catalyzed by a water-soluble fullerene-supported PdCl2 nanocatalyst
Liu, Wanyun,Zhou, Xiuming,Huo, Ping,Li, Jingbo,Mei, Guangquan
, p. 50 - 52 (2019/06/21)
A green synthesis of variously substituted biphenyl carboxylic acids was achieved through Suzuki–Miyaura cross-coupling of a bromobenzoic acid with an aryl boronic acid using a water-soluble fullerene-supported PdCl2 nanocatalyst (C60-TEGs/ PdCl2). Yields of more than 90% were obtained at room temperature in 4 h using 0.05 mol% catalyst and 2 equiv. K2CO3.
Palladium charcoal-catalyzed, ligandless Suzuki reaction by using tetraarylborates in water
Lu, Gang,Franzén, Robert,Zhang, Qian,Xu, Youjun
, p. 4255 - 4259 (2007/10/03)
In water and without using any ligand, palladium charcoal-catalyzed Suzuki coupling reaction of tetraarylborates with aryl bromides could be achieved in excellent yield. A concise mechanism consisting of four catalytic cycles is depicted in this paper.
