114772-78-0 Usage
Description
(4'-METHYL-1,1'-BIPHENYL-2-YL)METHANOL, with a molecular formula C14H14O, is a white crystalline solid that serves as a versatile precursor in the synthesis of pharmaceuticals and organic compounds. This chemical compound has demonstrated potential biological activity and is under investigation for its possible applications in medicine. Additionally, it is utilized in the production of dyes, pigments, and other industrial chemicals. However, due to its potential hazardous properties, it is crucial to handle this compound with care to avoid skin, eye, and respiratory irritation.
Uses
Used in Pharmaceutical Industry:
(4'-METHYL-1,1'-BIPHENYL-2-YL)METHANOL is used as a chemical precursor for the synthesis of various pharmaceuticals, contributing to the development of new medications and therapeutic agents.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, (4'-METHYL-1,1'-BIPHENYL-2-YL)METHANOL is employed as a starting material for the creation of diverse organic compounds, expanding the scope of chemical research and applications.
Used in Dye and Pigment Production:
(4'-METHYL-1,1'-BIPHENYL-2-YL)METHANOL is utilized as a key component in the manufacturing process of dyes and pigments, playing a significant role in the coloration and appearance of various products.
Used in Industrial Chemicals:
(4'-METHYL-1,1'-BIPHENYL-2-YL)METHANOL is also used in the production of other industrial chemicals, highlighting its versatility and importance in various chemical processes and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 114772-78-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,7,7 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 114772-78:
(8*1)+(7*1)+(6*4)+(5*7)+(4*7)+(3*2)+(2*7)+(1*8)=130
130 % 10 = 0
So 114772-78-0 is a valid CAS Registry Number.
114772-78-0Relevant articles and documents
A new vinyl ether type linker for solid-phase synthesis
Yoo,Gong,Choi,Seo,Kyu Yang Yi
, p. 6415 - 6418 (2000)
A new vinyl ether type of linker based on 4.-hydroxy phenethyl alcohol is developed for the solid-phase synthesis as demonstrated in the Suzuki type of aryl-aryl coupling reaction for the preparation of various biphenyl tetrazole derivatives. (C) 2000 Elsevier Science Ltd.
6-Arylphenanthridines from Aryl o-Biaryl Ketones with 1,1,1,3,3,3-Hexamethyldisilazane and Molecular Iodine
Kobayashi, Eiji,Kishi, Atsushi,Togo, Hideo
, p. 7335 - 7347 (2019/11/22)
Warming treatment of aryl o-biaryl ketones with 1,1,1,3,3,3-hexamethyldisilazane in the presence of Sc(OTf)3 in toluene, followed by the reaction with molecular iodine and K2CO3 in a mixture of THF and methanol at 60 °C gave the corresponding 6-arylphenanthridines in good to moderate yields. The present reaction is a one-pot method for the preparation of 6-arylphenanthridines from aryl o-biaryl ketones through the cyclization of imino-nitrogen-centered radicals that were generated from N-iodo aryl o-biaryl ketimines formed from the reaction of aryl biaryl ketimines with molecular iodine.
Intramolecular Acylation of Unactivated Pyridines or Arenes via Multiple C-H Functionalizations: Synthesis of All Four Azafluorenones and Fluorenones
Laha, Joydev K.,Jethava, Krupal P.,Patel, Sagarkumar,Patel, Ketul V.
, p. 76 - 85 (2017/04/26)
An unprecedented intramolecular acylation of unactivated pyridines via multiple C(sp3/sp2)-H functionalizations of a methyl, hydroxymethyl, or aldehyde group has been developed providing a general access to all four azafluorenones. The application of this protocol is further demonstrated to the synthesis of azafluorenone related fused nitrogen heterocycles and fluorenones. In addition, design and synthesis of a novel fluorene based organic emitter for potential use in organic light emitting devices (OLEDs) is also reported.
