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4,4-dichloro-2-phenyl-1-butene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20020-56-8

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20020-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20020-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,2 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20020-56:
(7*2)+(6*0)+(5*0)+(4*2)+(3*0)+(2*5)+(1*6)=38
38 % 10 = 8
So 20020-56-8 is a valid CAS Registry Number.

20020-56-8Relevant academic research and scientific papers

Copper-catalyzed formylation of alkenyl C-H bonds using BrCHCl2 as a stoichiometric formylating reagent

Bao, Yan,Wang, Gao-Yin,Zhang, Ya-Xuan,Bian, Kang-Jie,Wang, Xi-Sheng

, p. 2986 - 2990 (2018/03/23)

The first example of copper-catalyzed direct formylation of alkenyl C-H bonds for the facile synthesis of α,β-unsaturated aldehydes has been developed. This transformation has demonstrated high reactivity, mild reaction conditions and a broad substrate scope. BrCHCl2 is expected to be developed as an efficient stoichiometric C1 building block in organic synthesis.

A half-sandwich 1,2-azaborolyl ruthenium complex: Synthesis, characterization, and evaluation of its catalytic activities

Liu, Zicheng,Xu, Junjie,Ruan, Wenqing,Fu, Chen,Zhang, Hui-Jun,Wen, Ting-Bin

supporting information, p. 11976 - 11980 (2013/09/02)

A half-sandwich 1,2-azaborolyl (Ab) ruthenium complex, (Ab-CCPh) RuCl(PPh3)2 (1), has been synthesized by treating RuCl2(PPh3)3 with lithium 1,2-azaborolide L-1, or by treating either RuCl2(PPh3)3 or RuHCl(PPh3)3 directly with 1,2-azaborole LH-1. It is evaluated as a suitable precatalyst in [2 + 2] cycloadditions of norbornene derivatives with DMAD and in atom transfer radical additions of halogenated compounds with olefins. The Royal Society of Chemistry.

Preparation of Various 1,1-Dihalo-2-haloalkylcyclopropanes and 1,1,2-Trihalocyclopropanes and their Reduction to Dihalides using Tributyltin Hydride

Pettersen, Anita,Jorgensen, Evy,Sydnes, Leiv K.

, p. 603 - 609 (2007/10/02)

The title compounds, most of which were obtained by dihalocarbene addition to the corresponding alkenes, are generally reduced to dihalides in good yields. 1,1-Dichloro-2-chloromethyl-2-methylcyclopropane and all the tribromides investigated are attacked regioselectively at the gem-dihalo moiety, yielding isomeric mixtures of 1-halo-2-haloalkylcyclopropanes.Trihalides containing both bromo and chloro substituents are always attacked at the C-Br bond; as a consequence substituted 2-bromomethyl-1,1-dichlorocyclopropanes undergo ring opening and form 4,4-dichloro-1-butene derivatives.

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