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274924-71-9

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274924-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 274924-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,4,9,2 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 274924-71:
(8*2)+(7*7)+(6*4)+(5*9)+(4*2)+(3*4)+(2*7)+(1*1)=169
169 % 10 = 9
So 274924-71-9 is a valid CAS Registry Number.

274924-71-9Relevant articles and documents

Nucleophilic Substitution in 4-Bromo-5-nitrophthalodinitrile: XVI.1 4-(1H-Benzotriazol-1-yl)-5-[(4-carboxyphenyl)oxy/sulfanyl]- phthalonitriles and Cobalt Phthalocyanines Thereof

Znoiko,Kuz’min,Tikhomirova,Smirnov,Maizlish,Vashurin,Shaposhnikov

, p. 751 - 757 (2018)

A method of synthesis of 4-(1H-benzotriazol-1-yl)-5-[(4-carboxyphenyl)oxy]- and -5-[(4-carboxyphenyl) sulfanyl]phthalonitriles starting with 4-bromo-5-nitrophthalonitriles was developed. The synthesized phthalonitriles were used to prepare cobalt tetra-4-(1H-benzotriazol-1-yl)-tetra-5-[(4-carboxyphenyl)oxy/sulfanyl]phthalocyanines. The spectral and catalytic properties of the resulting octasubstituted phthalocyanines were studied.

Nucleophilic substitution in 4-bromo-5-nitrophthalodinitrile: XI. Preparation, properties, and prediction of mesomorphism in mixed-substituted phthalocyanines containing aryloxy and benzotriazole fragments

Znoiko,Akopova,Bumbina,Usoltseva,Maizlish,Shaposhnikov,Abramov

, p. 708 - 714 (2014/06/09)

Stepwise nucleophilic substitution of bromine and nitro group in 4-bromo-5-nitrophthalodinitrile has led to a series of phthalonitriles containing benzotriazole and aryloxy fragments; basing on them, the mixed-substituted phthalocyanines have been prepare

4-(1-Benzotriazolyl)-5-nitrophthalonitrile as a highly active substrate in aromatic nucleophilic substitution reactions

Smirnov, Alexey V.,Abramov, Igor G.,Plakhtinskii, Vladimir V.,Krasovskaya, Galina G.

, p. 72 - 74 (2007/10/03)

The title compound was synthesised, and its derivatives were prepared in high yields using the selective substitution of O-, S- and N-nucleophiles for the nitro group; an activating effect of the benzotriazolyl moiety on the above reactions was found.

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