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69142-93-4

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69142-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69142-93-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,4 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69142-93:
(7*6)+(6*9)+(5*1)+(4*4)+(3*2)+(2*9)+(1*3)=144
144 % 10 = 4
So 69142-93-4 is a valid CAS Registry Number.

69142-93-4Relevant articles and documents

A straightforward synthesis of symmetrical polyendiynes by dimerization reactions of silyl derivatives

Babudri, Francesco,Fiandanese, Vito,Marchese, Giuseppe,Punzi, Angela

, p. 251 - 257 (1998)

A straightforward synthesis of polyendiynes is described. The method is based upon a simple dimerization reaction of silylated enynes in the presence of copper salts. A variety of polyunsaturated compounds have been obtained in high yields and with high retention of configuration.

Ligand-free synthesis of 1,4-disubstituted-1,3-diynes by iron/copper cocatalyzed homocoupling of terminal alkynes

Wang, Peipei,Liu, Xiaoyan,Zhang, Songlin

, p. 187 - 194 (2013/08/24)

A simple and efficient protocol for Fe/Cu cocatalyzed oxidative homocoupling reaction of terminal alkynes to symmetrical 1,4-disubstituted-1,3- diynes was presented. The results showed that both CuBr and FeCl3 played crucial roles in the reaction. It is noteworthy that this protocol employs mild, efficient, aerobic and ligand free conditions. The alkynes, including aromatic, heteroaromatic and aliphatic alkynes, were transformed into the corresponding 1,3-diynes in good to excellent yields. A simple and efficient protocol for Fe/Cu cocatalyzed oxidative homocoupling reaction of terminal alkynes to symmetrical 1,4-disubstituted-1,3-diynes was presented. The results showed that both CuBr and FeCl3 played crucial roles in the reaction. It is noteworthy that this protocol employs mild, efficient, aerobic and ligand free conditions. The alkynes, including aromatic, heteroaromatic and aliphatic alkynes, were transformed into the corresponding 1,3-diynes in good to excellent yields. Copyright

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