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Piperazine, 1-(2-chloroethyl)-4-[(4-methylphenyl)sulfonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53727-44-9

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53727-44-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53727-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,2 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 53727-44:
(7*5)+(6*3)+(5*7)+(4*2)+(3*7)+(2*4)+(1*4)=129
129 % 10 = 9
So 53727-44-9 is a valid CAS Registry Number.

53727-44-9Downstream Products

53727-44-9Relevant academic research and scientific papers

Synthesis of sulfonamides: Via copper-catalyzed oxidative C-N bond cleavage of tertiary amines

Ji, Jing,Liu, Zhengyi,Liu, Ping,Sun, Peipei

, p. 7018 - 7023 (2016)

A copper-catalyzed coupling reaction of sulfonyl chlorides with tertiary amines via the oxidative C-N bond cleavage of tertiary amines was developed. Sulfonamides were synthesized using this strategy in moderate to good yields. The reaction was applicable to various tertiary amines, as well as sulfonyl chlorides.

Sulfonylation of 1,4-Diazabicyclo[2.2.2]octane: Charge-Transfer Complex Triggered C?N Bond Cleavage

Fu, Ying,Xu, Qin-Shan,Li, Quan-Zhou,Li, Ming-Peng,Shi, Chun-Zhao,Du, Zhengyin

, p. 127 - 131 (2019/02/06)

A novel charge-transfer complex triggered sulfonylation of 1,4-diazabicyclo[2.2.2]octane (DABCO) with mild reaction conditions has been developed. The formation of a charge-transfer complex between electron-withdrawing (hetero)aryl sulfonyl chloride and D

1,4-Diazabicyclo[2.2.2]octane (DABCO)- an efficient reagent in the synthesis of alkyl tosylates or sulfenates

Hartung, Jens,Huenig, Siegfried,Kneuer, Rainer,Schwarz, Michaela,Wenner, Hermann

, p. 1433 - 1438 (2007/10/03)

The bieyclic tertiary amine 1,4-diazabicyclo[2.2.2]octane (DABCO) is 8 promising substitute not only for the widely used but hazardous and hygroscopic base pyridine in the syntheses of alkyl tosylates 3 but also for triethylamine in the preparation of alk

Oligoethylenepiperazines

-

, (2008/06/13)

Oligoethylenepiperazines and their derivatives of the formula SPC1 Wherein n is a positive integer of 1 to 7 inclusive; m is zero or one when n=1, or m is one when n=2?7 R1 is hydrogen, benzenesulfonyl or benzenesulfonyl ring substituted by at least one member selected from the group consisting of lower alkyl of 1-4 carbon atoms, nitro and amino; R2 is halogen when m=zero and hydrogen, benzenesulfonyl or benzenesulfonyl ring substituted by at least one member selected from the group consisting of lower alkyl of 1-4 carbon atoms, nitro and amino when m=one; and the cationic salts thereof are useful as anion exchange oligomers, antihelmintic compounds, and intermediates for the preparation of polymers and fine industrial chemicals.

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