61593-02-0 Usage
Description
(2-Bromophenyl)diphenylmethanol, also known as bromodiphenylmethanol, is an organic compound with the molecular formula C19H15BrO. It is a white to off-white solid, and its structure consists of a central diphenylmethanol core with a bromine-substituted phenyl group. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and materials. Its properties make it a versatile building block for various organic synthesis processes.
Uses
Used in Pharmaceutical Industry:
(2-Bromophenyl)diphenylmethanol is used as an intermediate in the synthesis of pharmaceuticals for its versatility as a building block in organic synthesis processes.
Used in Agrochemical Industry:
(2-Bromophenyl)diphenylmethanol is used as an intermediate in the synthesis of agrochemicals for its potential to be incorporated into various chemical structures.
Used in Materials Industry:
(2-Bromophenyl)diphenylmethanol is used as an intermediate in the synthesis of materials for its ability to be a versatile component in creating new materials.
Used in Suzuki-Miyaura Coupling Reactions:
(2-Bromophenyl)diphenylmethanol is used as a reagent in Suzuki-Miyaura coupling reactions for its ability to facilitate the formation of carbon-carbon bonds.
Used in Negishi Coupling Reactions:
(2-Bromophenyl)diphenylmethanol is used as a reagent in Negishi coupling reactions for its role in promoting the coupling of organic fragments.
Used in Production of Cholesteric Liquid Crystals:
(2-Bromophenyl)diphenylmethanol is used in the production of cholesteric liquid crystals for its contribution to the formation of these specialized materials.
Check Digit Verification of cas no
The CAS Registry Mumber 61593-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,9 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61593-02:
(7*6)+(6*1)+(5*5)+(4*9)+(3*3)+(2*0)+(1*2)=120
120 % 10 = 0
So 61593-02-0 is a valid CAS Registry Number.
61593-02-0Relevant articles and documents
Evidence for Halogen Bonding in Amorphous Solid Dispersions
Deac, Alexandru,Gao, Yi,Indulkar, Anura S.,Mo, Huaping,Qi, Qingqing,Que, Chailu,Taylor, Lynne S.,Zeller, Matthias,Zemlyanov, Dmitry Y.,Zhang, Geoff G. Z.
, p. 3224 - 3235 (2020/05/27)
Carbon-bound halogen atoms (iodine, bromine, chlorine, and occasionally fluorine) are known to act as electron acceptors and form interactions with different species capable of acting as electron donors. This interaction is termed halogen bonding and shar
Synthesis, Coordination Properties, and Catalytic Application of Triarylmethane-Monophosphines
Iwai, Tomohiro,Tanaka, Ryotaro,Sawamura, Masaya
, p. 3959 - 3969 (2016/12/22)
A new class of triarylmethane-based phosphines (L1-L4) and their Pd(II) and Rh(I) complexes were synthesized and subsequently characterized by NMR spectroscopy and X-ray diffraction analysis. The reactions of these phosphines with [PdCl(π-allyl)]2 gave the square-planar Pd(II) complexes [PdCl(π-allyl)(L)] (L = L1-L4). The treatment of [PdCl(π-allyl)(L3)] and [PdCl(π-allyl)(L4)], which have CF3-substituted triarylmethane and 9-arylfluorene moieties, respectively, with LiOtBu afforded P,C(sp3)-chelated palladacycle complexes. Reversibility between a C(sp3)-M covalent bond and a C(sp3)-H···M interaction was experimentally demonstrated using [RhCl(nbd)]2 as a Rh(I) source. The triarylmethane-monophosphines L1-L4 were applied to the Pd-catalyzed 1,4-addition of arylboronic acids to enones.
Chiral allene-containing phosphines in asymmetric catalysis
Cai, Feng,Pu, Xiaotao,Qi, Xiangbing,Lynch, Vincent,Radha, Akella,Ready, Joseph M.
supporting information; experimental part, p. 18066 - 18069 (2012/01/04)
We demonstrate that allenes, chiral 1,2-dienes, appended with basic functionality can serve as ligands for transition metals. We describe an allene-containing bisphosphine that, when coordinated to Rh(I), promotes the asymmetric addition of arylboronic ac
