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2-hexyl-3-phenylbuta-1,3-diene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145642-48-4

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145642-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145642-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,6,4 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 145642-48:
(8*1)+(7*4)+(6*5)+(5*6)+(4*4)+(3*2)+(2*4)+(1*8)=134
134 % 10 = 4
So 145642-48-4 is a valid CAS Registry Number.

145642-48-4Downstream Products

145642-48-4Relevant academic research and scientific papers

Synthesis of 1,1,4,4-tetrabromo-2-butenes and related compounds via desilylation-bromination of silylated 1,3-butadiene derivatives

Xi, Zhenfeng,Liu, Xiaozhong,Lu, Jianming,Bao, Fengyu,Fan, Hongtao,Li, Zhiping,Takahashi, Tamotsu

, p. 8547 - 8549 (2004)

The combination of zirconocene-mediated coupling of silylated alkynes with a protonation-desilylation or bromination-desilylation process afforded otherwise unavailable butadiene derivatives. When (E,E)-2,3-dialkyl-1,4- bis(trimethylsilyl)-1,3-butadienes were treated with 3 equiv of Br2 in CH2Cl2, (E)-2,3-dialkyl-1,1,4,4-tetrabromo-2-butenes were obtained in excellent yields with perfect stereoselectivity.

Synthesis of multisubstituted 1,3-butadienes using the ruthenium-catalysed double addition of trimethylsilyldiazomethane to alkynylboronates

Morita, Ryotaro,Shirakawa, Eiji,Tsnchimoto, Teruhisa,Kawakami, Yusuke

, p. 1263 - 1268 (2007/10/03)

The ruthenium-catalysed double addition of trimethylsilyldiazomethane to alkynes developed by Dixneuf and co-workers was applied to the synthesis of 2-alkyl- or 2-aryl-3-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)1,4- bis(trimethylsilyl)-1,3-butadienes

One-pot conversion of terminal alkynes into gem-disubstituted-alkenes

Luo, Fen-Tair,Fwu, Shiang-Long,Huang, Wen-Shu

, p. 6839 - 6840 (2007/10/02)

A one-pot reaction of terminal alkynes with in situ generated hydrogen iodide and organozinc compounds in the presence of Pd(PPh3)4 provided a simple and useful method for the preparation of gem-disubstituted-alkenes.

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