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(3-butenyl)diphenylphosphine-borane complex is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127686-64-0

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127686-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127686-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,6,8 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 127686-64:
(8*1)+(7*2)+(6*7)+(5*6)+(4*8)+(3*6)+(2*6)+(1*4)=160
160 % 10 = 0
So 127686-64-0 is a valid CAS Registry Number.

127686-64-0Relevant academic research and scientific papers

Intramolecular hydroboration of unsaturated phosphine boranes

Shapland, Peter,Vedejs, Edwin

, p. 4094 - 4100 (2007/10/03)

Homoallylic phosphine boranes undergo intramolecular hydroboration upon activation by triflic acid. The reaction occurs via an intermediate B- trifluorosulfonyloxyborane complex such as 15, followed by SN1-like or SN2-like displaceme

Synthesis and structure of cyclic phosphine-boranes

Schmidbaur, Hubert,Sigl, Marcus,Schier, Annette

, p. 323 - 327 (2007/10/03)

In a search for cyclic phosphine-boranes, which can be expected to undergo ring opening polymerisation, or decomposition, to leave boron phosphide, the hydroboration reaction of ω-alkenyl-diphenylphosphines with boranes was investigated. Addition of one e

Synthesis and reactions of phosphine-boranes. Synthesis of new bidentate ligands with homochiral phosphine centers via optically pure phosphine-boranes

Imamoto, Tsuneo,Oshiki, Toshiyuki,Onozawa, Takashi,Kusumoto, Tetsuo,Sato, Kazuhiko

, p. 5244 - 5252 (2007/10/02)

Secondary and tertiary phosphine-boranes were synthesized in one-pot from phosphine oxides or substituted chlorophosphines without isolation of the intermediate phosphines. Phosphine-boranes having a methyl group were metalated with sec-butyllithium. The generated carbanions reacted with alkyl halides or carbonyl compounds to yield various phosphine-borane derivatives. The carbanions underwent copper(II)-promoted oxidative coupling without impairment of the borane functionality. Secondary phosphine-boranes reacted with alkyl halides, aldehydes, or α,β-unsaturated carbonyl compounds to give phosphine-borane derivatives having a functional group. The boranato group of phosphine-boranes was removed in a stereospecific manner with retention of configuration by treatment with a large excess of amine such as morpholine. A new route to bidentate ligands with homochiral phosphine centers has been explored by utilizing these characteristic reactivities of phosphine-boranes. Thus, optically pure (S,S)-1,2-bis(o-anisylphenylphosphino)ethane, (R,R)-1,2-bis(tert-butylphenyl-phosphino)ethane, and (S,S)-1,4-bis(o-anisylphenylphosphino)butane have been synthesized via phosphine-boranes.

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