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(+)-(2S,3R)-3-methyl-2-phenyl-4-penten-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

745813-63-2

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745813-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 745813-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,5,8,1 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 745813-63:
(8*7)+(7*4)+(6*5)+(5*8)+(4*1)+(3*3)+(2*6)+(1*3)=182
182 % 10 = 2
So 745813-63-2 is a valid CAS Registry Number.

745813-63-2Relevant academic research and scientific papers

Cu-catalyzed chemoselective preparation of 2-(pinacolato)boron-substituted allylcopper complexes and their insitu site-, diastereo-, and enantioselective additions to aldehydes and ketones

Meng, Fanke,Jang, Hwanjong,Jung, Byunghyuck,Hoveyda, Amir H.

supporting information, p. 5046 - 5051 (2013/07/05)

Sustainable, efficient, selective: A three-component, single-vessel Cu-catalyzed method for chemo-, diastereo-, and enantioselective conversion of B2(pin)2, monosubstituted allenes, and aldehydes or ketones to 2-B(pin)-substituted homoallylic alkoxides is described. Subsequent functionalization delivers valuable products in up to >98:2 d.r. and 97:3 e.r. (see scheme). Copyright

The mechanism and an improved asymmetric allylboration of ketones catalyzed by chiral biphenols

Barnett, David S.,Moquist, Philip N.,Schaus, Scott E.

supporting information; experimental part, p. 8679 - 8682 (2010/02/28)

Giving it a boost: A mechanistic study of the enantioselective asymmetric titled reaction with allyldiisopropoxyborane catalyzed by chiral biphenols revealed a key ligand exchange process which liberates isopropyl alcohol. The addition of iPrOH to the rea

Asymmetric allylboration of ketones catalyzed by chiral diols

Lou, Sha,Moquist, Philip N.,Schaus, Scott E.

, p. 12660 - 12661 (2008/02/05)

Chiral BINOL-derived diols catalyze the enantioselective asymmetric allylboration of ketones. The reaction requires 15 mol % of 3,3′-Br2-BINOL as the catalyst and allyldiisopropoxyborane as the nucleophile. The reaction products are obtained in

Silver-catalyzed asymmetric Sakurai-Hosomi allylation of ketones

Wadamoto, Manabu,Yamamoto, Hisashi

, p. 14556 - 14557 (2007/10/03)

The complex of AgF and (R)-DIFLUORPHOS has been shown to be an effective catalyst for the asymmetric Sakurai-Hosomi allylation of simple ketones. A significaant improvement of the reactivity was observed by using THF as the solvent. The catalyst turnover

Catalytic enantioselective allylboration of ketones

Wada, Reiko,Oisaki, Kounosuke,Kanai, Motomu,Shibasaki, Masakatsu

, p. 8910 - 8911 (2007/10/03)

The first example of catalytic enantioselective allylboration and crotylboration of simple ketones is described. High enantioselectivity (up to 93% ee) was obtained using 3 mol % CuF-iPr-DuPHOS as a chiral catalyst and 4.5 mol % La(Oi/sup

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