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1-biphenyl-4-yl-3-phenyl-prop-2-yn-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

478282-10-9

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478282-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 478282-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,2,8 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 478282-10:
(8*4)+(7*7)+(6*8)+(5*2)+(4*8)+(3*2)+(2*1)+(1*0)=179
179 % 10 = 9
So 478282-10-9 is a valid CAS Registry Number.

478282-10-9Relevant academic research and scientific papers

Ti-catalyzed regioselective ring-opening alkynylation of epoxides with haloalkynes

Zhang, Di,Li, Hao,Yi, Dong,Tu, Shijing,Qi, Zhongyu,Wei, Siping,Fu, Qiang,Fu, Haiyan,Du, Xi

supporting information, (2021/11/01)

Ti-catalyzed ring-opening alkynylation of epoxides with haloalkynes has been achieved, allowing an efficient and regioselective entry to various propargylic alcohols in moderate to good yields. The developed protocol features extremely mild reaction conditions, broad substrate scope, varied functional group compatibility, and chemospecificity in the rearrangements of epoxides to aldehydes.

Formation of α-lithio siloles from silylated 1,4-dilithio-1,3- butadienes: Mechanism and applications

Luo, Qian,Wang, Chao,Gu, Li,Zhang, Wen-Xiong,Xi, Zhenfeng

scheme or table, p. 1120 - 1128 (2011/07/09)

A full account of a useful transformation from silylated 1,4-dili-thio-1,3-butadienes to α-lithio siloles is described. These lithio siloles formed by this procedure are general, in terms of substitution patterns and synthetic methods, affording diversified silole derivatives. Notably, some structurally complex molecules, such as bridged bis-silole compounds, have been synthesized easily and successfully by applying our protocol. The structure of the α-lithio silole, which adopts a dimeric fashion through two lithium bridges, was confirmed by X-ray analysis. Furthermore, a possible mechanism of the skeleton rearrangements via E/Z isomerization of 1-silyl-1-lithio alkene and nucleophilic attack on silicon is proposed, and is also proved by experimental investigations. 2010 Wiley-VCH Verlag GmbH Co. KGaA, Weinheim.

Synthesis of functionalized siloles from Si-tethered diynes

Luo, Qian,Gu, Li,Wang, Chao,Liu, Junhui,Zhang, Wenxiong,Xi, Zhenfeng

supporting information; experimental part, p. 3213 - 3215 (2009/08/17)

A new synthetic itinerary to silole from Si-tethered diynes is reported. In this protocol, the Si-tethered diyne manifests definitely the reactivity of monoyne to form the lithio silole via zirconacyclopetadiene, 1,4-diiodo-1,3-butadiene, and the correspo

Optical behaviors of conjugated-chain compounds containing benzene and furan units

Pan, Wen-Long,Song, Ji-Guo,Chen, Yong,Wan, Yi-Qian,Song, Hua-Can

, p. 1300 - 1306 (2008/02/03)

Thirteen conjugated-chain compounds which contain benzene and furan units were prepared, their optical behaviors, including UV-vis absorption coefficient (ε), absorption wavelengths (λa), fluorescence emission wavelengths (λe), and q

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