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Benzene, (2-methyl-1,3-butadienyl)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39600-68-5

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39600-68-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39600-68-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,0 and 0 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39600-68:
(7*3)+(6*9)+(5*6)+(4*0)+(3*0)+(2*6)+(1*8)=125
125 % 10 = 5
So 39600-68-5 is a valid CAS Registry Number.

39600-68-5Downstream Products

39600-68-5Relevant academic research and scientific papers

Stereoselective Synthesis of Terminal 1,3-Butadienes by the Condensation Reaction of Aldehydes and Ketones with the γ-Trimethylsilyl-Substituted Allylboranes

Wang, Kung K.,Liu, Chin,Gu, Yu Gui,Burnett, Friedrich N.,Sattsangi, Prem D.

, p. 1914 - 1922 (2007/10/02)

Allylboranes 7-12, readily prepared from allenylsilanes 1-6 by hydroboration with 9-borabicyclononane, smoothly condense with aldehydes and ketones to afford, after basic or acidic workup to promote the Peterson olefination reaction, a variety of t

Stereoselective Synthesis of (Z)- and (E)-1,3-Alkadienes from Aldehydes Using Organotitanium and Lithium Reagents

Ikeda, Yoshihiko,Ukai, Junzo,Ikeda, Nobuo,Yamamoto, Hisashi

, p. 723 - 730 (2007/10/02)

titanium reagent generated easily from allyldiphenylphosphine condenses with aldehydes to give (Z)-1,3-alkadienes in a highly regio- and stereoselective manner.In contrast, lithiated allyldiphenylphosphine oxide condenses with aldehydes to give (E)-1,3-alkadienes directly and stereoselectively in good yield.Similarly, lithiated (1-buten-3-yl)diphenylphosphine oxide condenses with aldehydes to give (E)-3-methyl-1,3-alkadienes.

DIRECT, STEREOSELECTIVE SYNTHESIS OF EITHER E- OR Z-1,3-DIENES

Ukai, Junzo,Ikeda, Yoshihiko,Ikeda, Nobou,Yamamoto, Hisashi

, p. 4029 - 4032 (2007/10/02)

New synthetic methods for the preparation of Z- or E-1,3-dienes are described.

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