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5-Hexenoic acid, 4-methyl-, phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138174-31-9

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138174-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138174-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,7 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138174-31:
(8*1)+(7*3)+(6*8)+(5*1)+(4*7)+(3*4)+(2*3)+(1*1)=129
129 % 10 = 9
So 138174-31-9 is a valid CAS Registry Number.

138174-31-9Downstream Products

138174-31-9Relevant academic research and scientific papers

Substituted butenylindium generated by transmetalation of cyclopropylmethylstannane with indium iodide: Synthesis and characterization of monobutenylindium

Kiyokawa, Kensuke,Yasuda, Makoto,Baba, Akio

scheme or table, p. 2039 - 2043 (2011/06/18)

Transmetalation between substituted cyclopropylmethylstannanes and indium iodide provided the corresponding mono- and dibutenylindium species. The bulky substituent on a cyclopropyl ring selectively afforded the monobutenylindium species, which allowed th

Preparation and Reactivities of (η3-1- and 2-Trimethylsiloxyallyl)Fe(CO2)NO Complexes. Intermediates Functioning as Equivalents of β- and α-Acyl Carbocations and Acyl Carbanions

Itoh, Keiji,Nakanishi, Saburo,Otsuji, Yoshio

, p. 2965 - 2977 (2007/10/02)

(η3-1- and 2-Trimethylsiloxyallyl)Fe(CO)2NO complexes were prepared by the reaction of the corresponding siloxyallylic halides with Bu4N.These complexes reacted with both of carbon nucleophiles and carbon electrophiles preferentially at the less hindered sites of the allylic ligands.In these reactions, (η3-1-trimethylsiloxyallyl)Fe(CO)2NO complexes served as synthetically equivalent synthons for both of β-acyl carbocations and β-acyl carbanions and (η3-2-trimethylsiloxyallyl)Fe(CO)2NO complexes as both of α-acyl carbocations and α-acyl carbanions.The stereochemical courses of the reactions are described.

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