143651-26-7 Usage
General Description
4-(Trans-4-Pentylcyclohexyl) Phenyl Boronic Acid is a synthetic compound belonging to the group of organic chemicals known as boronic acids. It is characterized by the presence of a boronic acid functional group (-B(OH)2). The primary use of this specific compound is not explicitly defined but boronic acids, in general, are used extensively in organic chemistry, particularly in the Suzuki reaction. This class of chemicals is often utilized as a versatile tool in the field of medicinal chemistry and drug discovery as well. However, detailed information regarding the safety, toxicity, and environmental impact of 4-(Trans-4-Pentylcyclohexyl) Phenyl Boronic Acid is not readily available.
Check Digit Verification of cas no
The CAS Registry Mumber 143651-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,6,5 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 143651-26:
(8*1)+(7*4)+(6*3)+(5*6)+(4*5)+(3*1)+(2*2)+(1*6)=117
117 % 10 = 7
So 143651-26-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H27BO2/c1-2-3-4-5-14-6-8-15(9-7-14)16-10-12-17(13-11-16)18(19)20/h10-15,19-20H,2-9H2,1H3/t14-,15-
143651-26-7Relevant articles and documents
Helical nylons and polyphthalamides synthesized by chiral interfacial polymerizations between chiral nematic liquid crystal and water layers
Park, Jinwoo,Goh, Munju,Akagi, Kazuo
, p. 2784 - 2795 (2014/06/09)
Polyamides are one of the most widely used engineering plastics. Aliphatic polyamide represented by nylon has been previously synthesized by an interfacial polymerization reaction between an organic layer of diacyl chloride and a water layer of diamine. H
