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1-iodo-4-methyl-2-(p-tolylethynyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1558818-52-2

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1558818-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1558818-52-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,5,8,8,1 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1558818-52:
(9*1)+(8*5)+(7*5)+(6*8)+(5*8)+(4*1)+(3*8)+(2*5)+(1*2)=212
212 % 10 = 2
So 1558818-52-2 is a valid CAS Registry Number.

1558818-52-2Downstream Products

1558818-52-2Relevant academic research and scientific papers

Copper-catalysed three-component carboiodination of arynes: Expeditious synthesis of: O -alkynyl aryl iodides

Cao, Wenxuan,Niu, Sheng-Li,Shuai, Li,Xiao, Qing

supporting information, p. 972 - 975 (2020/02/03)

A copper-catalysed three-component iodoalkynylation reaction of arynes for the expeditious and versatile synthesis of o-alkynyl aryl iodides has been developed. Mechanism research shows that the reaction goes through two steps enabled by copper catalysis: the formation of 1-iodo-2-arylacetylene and the insertion of the aryne into a C(sp)-I bond.

Diaceno[a,e]pentalenes from homoannulations of o-alkynylaryliodides utilizing a unique Pd(OAc)2/n-Bu4NOAc catalytic combination

Shen, Junjian,Yuan, Dafei,Qiao, Yan,Shen, Xingxing,Zhang, Zhongbo,Zhong, Yuwu,Yi, Yuanping,Zhu, Xiaozhang

, p. 4924 - 4927 (2015/04/27)

A heterogeneous catalytic system, Pd(OAc)2/n-Bu4NOAc, for the efficient synthesis of diaceno[a,e]pentalenes via a tandem Pd catalytic cycle is reported. The catalytic partner n-Bu4NOAc played indispensable and versatile ro

Synthesis of tetracyclic chromenones via platinum(ii) chloride catalysed cascade cyclization of enediyne-enones

Sivaraman, Mahalingam,Perumal, Paramasivan T.

, p. 1318 - 1327 (2014/03/21)

PtCl2 catalysed cascade cyclization of an enediyne-enone system to afford a tetracyclic chromenone is reported, which proceeds through two consecutive highly regioselective 6-endo-dig cyclizations in a single step with the formation of two new C-C bonds and two new rings in excellent yield. A mechanism for this transformation is proposed based on the isolated intermediates.

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