787618-25-1 Usage
Uses
Used in Pharmaceutical Synthesis:
[1,1-Biphenyl]-2,6-diol,2-bromo-(9CI) is used as a key intermediate in the synthesis of various pharmaceuticals for [application reason] its ability to participate in coupling reactions and functionalization processes, which enables the creation of a wide range of therapeutically relevant molecules.
Used in Agrochemical Synthesis:
In the agrochemical industry, [1,1-Biphenyl]-2,6-diol,2-bromo-(9CI) is used as a starting material for the development of new agrochemicals for [application reason] its reactivity and versatility in chemical reactions, which can lead to the production of innovative compounds with improved performance in agriculture.
Used in Chemical Research:
[1,1-Biphenyl]-2,6-diol,2-bromo-(9CI) is utilized as a research compound in the field of chemistry for [application reason] its unique structural features and reactivity, which make it an ideal candidate for studying various chemical reactions and exploring new synthetic pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 787618-25-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,7,6,1 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 787618-25:
(8*7)+(7*8)+(6*7)+(5*6)+(4*1)+(3*8)+(2*2)+(1*5)=221
221 % 10 = 1
So 787618-25-1 is a valid CAS Registry Number.
787618-25-1Relevant articles and documents
Isothiourea-Catalyzed Atropselective Acylation of Biaryl Phenols via Sequential Desymmetrization/Kinetic Resolution
Brueckner, Alexander C.,Campbell, Andrew D.,Cheong, Paul Ha-Yeon,Feoktistova, Taisiia,Grove, Markas A.,Munday, Elizabeth S.,Slawin, Alexandra M. Z.,Smith, Andrew D.,Walden, Daniel M.,Young, Claire M.
, p. 7897 - 7905 (2020/03/23)
Axially chiral phenols are attractive targets in organic synthesis. This motif is central to many natural products and widely used as precursors to, or directly, as chiral ligands and catalysts. Despite their utility few simple catalytic methods are avail
An extremely active catalyst for the Negishi cross-coupling reaction
Milne, Jacqueline E.,Buchwald, Stephen L.
, p. 13028 - 13032 (2007/10/03)
A new catalyst system for the Pd-catalyzed cross-coupling of organozinc reagents with aryl halides (Negishi coupling) has been developed. This system permits efficient preparation of hindered biaryls (triand tetra-ortho- substituted), functions effectively at low levels of catalyst, and tolerates a wide range of functional groups and heterocyclic substrates. A systematic study of ligand structure was performed and was correlated with catalyst activity.
