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1-O-(p-tolylsulfonyl)dodec-3-yn-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

125198-07-4

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125198-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125198-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,1,9 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 125198-07:
(8*1)+(7*2)+(6*5)+(5*1)+(4*9)+(3*8)+(2*0)+(1*7)=124
124 % 10 = 4
So 125198-07-4 is a valid CAS Registry Number.

125198-07-4Relevant academic research and scientific papers

Preparation of 2,3,4,5-tetrahydropyridines from 5-alkynylamines under the catalytic action of gold(III) salts

Fukuda,Utimoto

, p. 975 - 978 (1991)

Intramolecular addition of amine to carbon-carbon triple bonds in 5-alkynylamines produces 2,3,4,5-tetrahydropyridines under the catalytic action of an aurate salt. Some venom components of various ant species are synthesized by the application of this re

First Total Synthesis of Ganglioside GAA-7 from Starfish Asterias amurensis versicolor

Tamai, Hideki,Imamura, Akihiro,Ogawa, Junya,Ando, Hiromune,Ishida, Hideharu,Kiso, Makoto

, p. 5199 - 5211 (2015/08/18)

The first total synthesis of neuritogenic ganglioside GAA-7 was achieved using the glucosyl ceramide (Glc-Cer) cassette approach. The stereocenter triad within the ceramide moiety of the target molecule was efficiently established from D-lyxose. The assem

Palladium-Catalyzed Intramolecular Addition of Amines to Acetylenes. Synthesis of Cyclic Imines

Fukuda, Yukitoshi,Matsubara, Seijiro,Utimoto, Kiitiro

, p. 5812 - 5816 (2007/10/02)

Intramolecular aminopalladation of alkynylamines gave intermediary alkenylpalladium compounds that hydrolyzed and isomerized to thermodynamically stable cyclic imines.Treatment of 3-alkynylamines with a catalytic amount of PdCl2(MeCN)2 gave exclusively 1-

Design, Synthesis, and 5-Lipoxygenase-Inhibiting Properties of 1-Thio-Substiuted Butadienes

Hanko, Rudolf,Hammond, Michael D.,Fruchtmann, Romanis,Pfitzner, Joerg,Place, Graham A.

, p. 1163 - 1170 (2007/10/02)

The synthesis of novel 1-thio-substituted butadienes, designed as mechanism-based 5-lipoxygenase inhibitors, is described.The structure of these compounds closely resembles a proposed high-energy intermediate during the lipoxygenation of arachidonic acid.They demonstrate 5-lipoxygenase inhibition in vitro and in vivo.The most potent compound is 15a with an IC50 of μM in vitro.LTC4 release was inhibited by 80percent after intraperitoneal administration of 15c at a dose of 2 mg/kg.

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