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2-Propanesulfonic acid, phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25077-97-8

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25077-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25077-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,7 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 25077-97:
(7*2)+(6*5)+(5*0)+(4*7)+(3*7)+(2*9)+(1*7)=118
118 % 10 = 8
So 25077-97-8 is a valid CAS Registry Number.

25077-97-8Downstream Products

25077-97-8Relevant academic research and scientific papers

ALKANESULFONYLATION.XX. CATALYSIS OF THE PHENOLYSIS OF ALKANESULFONYL CHLORIDES IN PROTON-INERT MEDIA CATALYZED BY PYRIDINE BASES. THE EFFECT OF THE SUBSTRATE STRUCTURE

Skrypnik, Yu. G.,Lyashchuk, S. N.

, p. 695 - 700 (2007/10/02)

The kinetics of the reaction of methane-, ethane-, propane-, 1-methylmethane-, and cyclohexanesulfonyl chlorides and also of substituted phenylmethanesulfonyl chlorides with phenol in the presence of pyridine in chlorobenzene at 303 K were studied by GLC

Studies on the Base-catalyzed Solvolysis of Propane-2-sulphonic Acid p-Cresylester

Lehmann, Heinz,Pritzkow, Wilhelm

, p. 251 - 256 (2007/10/02)

Products of the reaction of propane-2-sulphonic acid p-cresylester with sodium butoxide in butanol are the sodium salt of propan-2-sulphonic acid, di-n-butyl ether, p-cresyl-n-butyl ether and p-cresol.The reaction proceeds via propane-2-sulphonic acid n-butylester which is formed from the starting compound by an elimination-addition (sulphene) mechanism.The elimination step is an E1-cB reaction.

ALKANESULFONYLATION REACTIONS. X. EFFECT OF THE STRUCTURE OF THE ALKANESULFONYL HALIDE ON THE FORMATION OF PHENYLALKANESULFONATES CATALYZED BY TRIETHYLAMINE

Bezrodnyi, V. P.,Skrypnik, Yu. G.

, p. 1660 - 1665 (2007/10/02)

The kinetics of the reactions of methane-, propane-, isopropane-, cyclohexane, and phenylmethanesulfonyl chlorides and propanesulfonyl bromide with phenol in the presence of triethylamine in benzene at 30 deg C were investigated by GLC and potentiometric

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