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diisopropyl (E)-(2-phenylprop-1-en-1-yl)phosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78462-99-4

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78462-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78462-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,6 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78462-99:
(7*7)+(6*8)+(5*4)+(4*6)+(3*2)+(2*9)+(1*9)=174
174 % 10 = 4
So 78462-99-4 is a valid CAS Registry Number.

78462-99-4Relevant academic research and scientific papers

Ag(I)-catalyzed synthesis of (E)-alkenyl phosphonates by oxidative coupling of H-phosphites with β-nitroolefins

Ma, Li,Shang, Shengjie,Yuan, Hua,Zhang, Yue,Zeng, Zhigang,Chen, Yunfeng

supporting information, (2021/11/17)

A novel reaction constructing C(sp2)-P bond via the silver-catalyzed polarity-matched oxidative coupling of various H-phosphites with β-alkyl nitroolefins has been achieved. The reaction was performed by using acetonitrile as the solvent and Ni(NO3)2·6H2O as the oxidant, which could restrain unwanted isomerization of β-nitroolefins and selective produce (E)-alkenyl phosphonates in up to 83% yield.

Inverting External Asymmetric Induction via Selective Energy Transfer Catalysis: A Strategy to β-Chiral Phosphonate Antipodes

Onneken, Carina,Bussmann, Kathrin,Gilmour, Ryan

supporting information, p. 330 - 334 (2019/12/11)

Enantiodivergent, catalytic reduction of activated alkenes relays stereochemical information encoded in the antipodal chiral catalysts to the pro-chiral substrate. Although powerful, the strategy remains vulnerable to costs and availability of sourcing bo

Copper-mediated selective cross-coupling of 1,1-dibromo-1-alkenes and heteronucleophiles: Development of general routes to heterosubstituted alkynes and alkenes

Jouvin, Kevin,Coste, Alexis,Bayle, Alexandre,Legrand, Frederic,Karthikeyan, Ganesan,Tadiparthi, Krishnaji,Evano, Gwilherm

, p. 7933 - 7947 (2013/01/16)

Efficient and general procedures for the cross-coupling of 1,1-dibromoalkenes and N-, O-, and P-nucleophiles are reported. Fine-tuning of the reaction conditions allows for either site-selective, double, or alkynylative cross-coupling, therefore providing

Copper-mediated cross-coupling of 1,1-dibromo-1-alkenes with dialkyl phosphites: A convenient synthesis of 1-alkenylphosphonates

Evano, Gwilherm,Tadiparthi, Krishnaji,Couty, Francois

supporting information; experimental part, p. 179 - 181 (2011/02/25)

An efficient and stereoselective procedure for the preparation of E-1-alkenylphosphonates by copper-mediated cross-coupling between 1,1-dibromo-1-alkenes and dialkyl phosphites is reported. The reaction allows for formal substitution of both bromine atoms

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