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3253-29-0

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3253-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3253-29-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,5 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3253-29:
(6*3)+(5*2)+(4*5)+(3*3)+(2*2)+(1*9)=70
70 % 10 = 0
So 3253-29-0 is a valid CAS Registry Number.

3253-29-0Downstream Products

3253-29-0Relevant articles and documents

Reaction of Dialkyl Dithiophosphates with Arylhydrazones of Mesoxalodinitrile and with Ethyl Cyanohydrazonoacetate

Rymareva,Torgasheva,Zelikhover,Bel'skii

, p. 1417 - 1423 (2007/10/03)

Dialkyl hydrogen dithiophosphates add in mild conditions to the nitrile group of arylhydrazones of mesoxalodinitrile and of ethyl cyanohydrazonoacetate to give 2-R-2-(arylhydrazono)-N-(dialkylphosphinothioyl)thioacetamides, 2-R-2-(arylhydrazono)-2-cyanoth

REACTION OF DIISOPROPYLDITHIOPHOSPHORIC ACID WITH BENZONITRILE IN THE PRESENCE OF A THIRD COMPONENT

Zabirov, N. G.,Shamsevaleev, F. M.,Cherkasov, R. A.

, p. 558 - 562 (2007/10/02)

Reaction in the three component systems nitrile-dithiophosphorus acid-phenol or carboxylic acid proceeds by three routes, all of which include the initial stage of formation of imidoyldithiophosphates.The latter forms stable products by isomerization with 1,3-S->N migration of the thiophosphoryl group and by decomposition under the influence of dithiophosphorus acids, phenol, or carboxylic acid.When aniline or methyl iodide is used as the third component the reaction proceeds by a different route and leads to the formation, respectively, of amidine dithiophosphate salts or a mixture of methylation products.

N,N'-BIS(1-CHLOROALKYL)CARBODIIMIDES. IV. REACTIONS WITH O,O-DIALKYL DITHIOPHOSPHITES

Fetyukhin, V. N.,Vovk, M. V.,Samarai, L. I.

, p. 571 - 573 (2007/10/02)

In a a number of cases the reaction of N,N'-bis(1-chloroalkyl)carbodiimides with O,O-dialkyl dithiophosphates takes place abnormally with retention of the carbodiimide structure in the reaction products.

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