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(Z)-4,8-dimethylnona-3,7-dienenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74582-94-8

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74582-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74582-94-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,8 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74582-94:
(7*7)+(6*4)+(5*5)+(4*8)+(3*2)+(2*9)+(1*4)=158
158 % 10 = 8
So 74582-94-8 is a valid CAS Registry Number.

74582-94-8Downstream Products

74582-94-8Relevant academic research and scientific papers

Cyanation of Allylic Carbonates and Acetates Using Trimethylsilyl Cyanide Catalyzed by Palladium Complex

Tsuji, Yasushi,Yamada, Naoaki,Tanaka, Shinsuke

, p. 16 - 17 (2007/10/02)

Allylic carbonates and acetates are cyanated with trimethylsilyl cyanide in the presence of a catalytic amount (5 mol percent based on the allylic substrates) od Pd(PPh3)4 or Pd(CO)(PPh3)3 in THF under reflux to afford β,γ-unsaturated nitriles in high yields.

Cyano Phosphate: An Efficient Intermediate for the Chemoselective Conversion of Carbonyl Compounds to Nitriles

Yoneda, Ryuji,Harusawa, Shinya,Kurihara, Takushi

, p. 1827 - 1832 (2007/10/02)

Cyanohydrin diethyl phosphates, readily obtained from various ketones and aldehydes by reaction with diethyl phosphorocyanidate and lithium cyanide, reacted chemoselectively with samarium(II) iodide in THF to give the corresponding nitriles in excellent yields.This method was also found applicable to α,β-unsaturated carbonyl compounds via cyano phosphates to give β,γ-unsaturated nitriles, not obtainable by standard methods, without isomerization of the double bonds.

Reaction of Allyl Diphenyl Phosphates with Soft Bases

Araki, Shuki,Minami, Kazuhiro,Butsugan, Yasuo

, p. 629 - 630 (2007/10/02)

The title phosphates were found to react with a variety of soft bases to give nucleophilic substitution products in high yields.The reaction proceeded regiospecifically under mild reaction conditions with preservation of the double bond geometry.

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