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1439362-64-7

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1439362-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1439362-64-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,9,3,6 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1439362-64:
(9*1)+(8*4)+(7*3)+(6*9)+(5*3)+(4*6)+(3*2)+(2*6)+(1*4)=177
177 % 10 = 7
So 1439362-64-7 is a valid CAS Registry Number.

1439362-64-7Downstream Products

1439362-64-7Relevant articles and documents

Combination of gold and iridium catalysts for the synthesis of N-alkylated amides from nitriles and alcohols

Li, Feng,Ma, Juan,Lu, Lei,Bao, Xiaofeng,Tang, Wanying

, p. 1953 - 1960 (2015)

An alternative and efficient approach for the synthesis of N-alkylated amides from nitriles and alcohols was proposed and accomplished. By the combination of [(IPr)Au(NTf2)] (IPr = 1,3-bis(diisopropylphenyl)imidazol-2-ylidene) and [CpIrCl2]2 (Cp = η5-pentamethylcyclopentadienyl), a series of nitriles were first hydrated to give amides, in which the resulting amides were further N-alkylated with a variety of alcohols as alkylating agents to afford N-alkylated amides with good to excellent yields. Compared with previous methods for the synthesis of N-alkylated amides from nitriles and alcohols as starting materials, this protocol could be accomplished with high atom economy under more environmentally benign conditions.

Method for synthesizing N-alkylamide

-

, (2016/12/07)

The invention discloses a method for synthesizing N-alkylamide. In a reaction container, adding nitrile, a complex of a transition-metal catalyst gold, a solvent tetrahydrofuran and H2O; reacting a reaction mixture for several hours at the temperature of 130-140 DEG C, cooling the reaction mixture to room temperature, performing vacuum pressure reduction to remove the solvent; adding a compound alcohol, alkali, the complex of a transition-metal catalyst iridium, a solvent toluene, reacting the reaction mixture for several hours at the temperature of 130 DEG C, through column separation, obtaining a target compound. According to the invention, with participation of the transition-metal catalyst, commercial nitrile is hydrolyzed to generate an amide intermediate, and then is subjected to an alkylation reaction with alcohol to obtain N-alkylamide. The reaction has three obvious advantages: 1) the commercial nitrile and alcohol which is almost nontoxic are taken as initial raw materials; 2) only water is generated as a by-product in the reaction, so that the reaction has no harm on environment; and 3) reaction atom economy is high. The reaction accords with green chemistry requirement, and has wide development prospect.

Tandem synthesis of N-alkylated amides from aldoximes and alcohols by using a Ru/Ir dual-catalyst system

Li, Feng,Qu, Panpan,Ma, Juan,Zou, Xiaoyuan,Sun, Chunlou

, p. 2178 - 2182 (2013/08/23)

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