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70443-66-2

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70443-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70443-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,4 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 70443-66:
(7*7)+(6*0)+(5*4)+(4*4)+(3*3)+(2*6)+(1*6)=112
112 % 10 = 2
So 70443-66-2 is a valid CAS Registry Number.

70443-66-2Relevant academic research and scientific papers

Preparation method for synthesizing ester compound by using N-Boc amide as raw material

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Paragraph 0041; 0042, (2019/03/28)

The invention relates to a preparation method for synthesizing an ester compound by using N-Boc amide as a raw material. According to the method, an inorganic base is used as a catalyst; the N-Boc amide is subjected to an intermolecular nucleophilic substitution reaction with various alcohol compounds; and various ester compounds can be efficiently obtained. The method has the advantages of beingmild in reaction condition, simple and convenient to operate, high in yield and favorable in functional-group compatibility.

Metal-free transesterification catalyzed by tetramethylammonium methyl carbonate

Hatano, Manabu,Tabata, Yuji,Yoshida, Yurika,Toh, Kohei,Yamashita, Kenji,Ogura, Yoshihiro,Ishihara, Kazuaki

supporting information, p. 1193 - 1198 (2018/03/27)

Environmentally benign metal-free tetramethylammonium methyl carbonate is effective as a catalyst for the chemoselective, scalable, and reusable transesterification of various esters and alcohols in common organic solvents. In situ-generated highly active species, tetramethylammonium alkoxides, can greatly avoid self-decomposition at ≤110 °C, and are reusable. In particular, chelating substrates, such as amino alcohols, diols, triols, sugar derivatives, alkaloids, α-amino acid esters, etc., which deactivate conventional metal salt catalysts, can be used. A 100 gram scale biodiesel production was also demonstrated.

Selective mono-acylation of 1,2- and 1,3-diols using (α,α- difluoroalkyl)amines

Wakita, Natsumi,Hara, Shoji

experimental part, p. 7939 - 7945 (2010/10/19)

In the reaction of N,N-diethyl-α,α-difluorobenzylamine (DFBA) with 1,2- or 1,3-diols, selective mono-benzoylation occurs to afford mono-esters of the diols in good yield. The reaction is completed under mild conditions in a short reaction time. Further, prim-, sec-, and tert-diols and catechol can be converted to the corresponding mono-benzoates. DFBA is used for the protection of the hydroxy group in sugars. The selective mono-nicotinylation, formylation and pivaloylation of diols are also performed by using the corresponding difluoroalkylamines.

One-pot preparation of esters from carboxylic acids using the PPh3-CCl3CN system

Jang, Doo Ok,Cho, Dae Hyan,Kim, Joong-Gon

, p. 2885 - 2890 (2007/10/03)

A convenient one-pot process for preparing various esters from carboxylic acids using the Ph3P-CCl3CN has been developed. Racemic α-tocopherol, clofibrate and flavoxate were prepared in high yields using this method.

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