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3-butyl-1-phenyl-1-heptyn-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

160006-19-9

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160006-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160006-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,0,0 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 160006-19:
(8*1)+(7*6)+(6*0)+(5*0)+(4*0)+(3*6)+(2*1)+(1*9)=79
79 % 10 = 9
So 160006-19-9 is a valid CAS Registry Number.

160006-19-9Relevant articles and documents

SmI2-mediated coupling reactions between iodoalkynes and ketones or aldehydes to give propargyl alcohols

Kunishima,Tanaka,Kono,Hioki,Tani

, p. 3707 - 3710 (1995)

Samarium iodide (SmI2) mediates a coupling reaction between alkynyl iodides and ketones or aldehydes to give propargyl alcohols in the presence of hexamethylphosphoric triamide (HMPA) in either benzene or tetrahydrofuran (THF). An alkynylsamari

Generation and reactions of alkynylsamariums

Kunishima, Munetaka,Nakata, Daisuke,Tanaka, Shinobu,Hioki, Kazuhito,Tani, Shohei

, p. 9927 - 9935 (2000)

Three methods have been developed for generating alkynylsamariums: (1) reduction of iodoalkynes with SmI2 in the presence of HMPA, (2) deprotonation at the terminal position of 1-alkynes either by tetrahydrofurylsamarium generated by PhI and Sm

Mild and solvent-free alkynylation of ketones on the KF/alumina

Sharifi, Ali,Mirzaei, Mojtaba,Naimi-Jamal, M. Reza

, p. 1039 - 1044 (2007/10/03)

The solvent-free alkynylation of various ketones on the surface of KF/alumina under mild conditions is described. Copyright Taylor & Francis, Inc.

Preparation of oxetanes by 4-endo trig electrophilic cyclisations of cinnamic alcohols

Albert, Sébastien,Robin, Sylvie,Rousseau, Gérard

, p. 2477 - 2479 (2007/10/03)

The reaction of substituted cinnamic alcohols with bis(sym-collidine)bromine(I) hexafluorophosphate was examined. In general no oxetane was obtained when a substituent was fixed on the carbon-carbon double bond. However, oxetanes were formed in high yield

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