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Benzaldehyde, 4-(6-hydroxy-1-hexynyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

679796-98-6

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679796-98-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 679796-98-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,9,7,9 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 679796-98:
(8*6)+(7*7)+(6*9)+(5*7)+(4*9)+(3*6)+(2*9)+(1*8)=266
266 % 10 = 6
So 679796-98-6 is a valid CAS Registry Number.

679796-98-6Relevant academic research and scientific papers

Coupling reactions of aryl bromides with 1-alkynols catalysed by a tetraphosphine/palladium catalyst

Feuerstein, Marie,Doucet, Henri,Santelli, Maurice

, p. 1603 - 1606 (2004)

cis,cis,cis-1,2,3,4-Tetrakis(diphenylphosphinomethyl)cyclopentane/ [PdCl(C3H5)]2 system catalyses efficiently the coupling reactions of aryl halides with a variety of alkynols such as propargyl alcohol, but-1-yn-4-ol, pent

Synthesis and spectral properties of fluorescent linear alkylphosphocholines labeled with all-(E)-1,6-diphenyl-1,3,5-hexatriene

Hornillos, Valentín,Tormo, Laura,Amat-Guerri, Francisco,Acu?a, A. Ulises

scheme or table, p. 79 - 84 (2011/02/22)

A synthetic method has been designed to produce alkylphosphatidylcholine lipid molecules with the fluorescent group all-(E)-1,6-diphenyl-1,3,5-hexatriene (DPH) incorporated to the end of a polymethylene chain of variable length. The resulting compounds ma

Efficient remote axial-to-central chirality transfer in enantioselective SmI2-mediated reductive coupling of aldehydes with crotonates of atropisomeric 1-naphthamides

Zhang, Yan,Wang, Yongqiang,Dai, Wei-Min

, p. 2445 - 2455 (2007/10/03)

Control of enantioselectivity by remote amide conformation has been studied in SmI2-mediated reductive coupling of aldehydes with the crotonates possessing different 2-substituted 8-methoxy-1-naphthamides. The enantiomers of atropisomeric 8-met

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