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methyl 8-chloro-2-(4-methoxyphenyl)-1,2,3,4-tetrahydroquinoline-6-acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

149264-77-7

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149264-77-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 149264-77-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,2,6 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 149264-77:
(8*1)+(7*4)+(6*9)+(5*2)+(4*6)+(3*4)+(2*7)+(1*7)=157
157 % 10 = 7
So 149264-77-7 is a valid CAS Registry Number.

149264-77-7Downstream Products

149264-77-7Relevant academic research and scientific papers

Synthesis and antirheumatic activity of novel tetrahydro-6-quinolineacetic acid derivatives

Kohno, Yasushi,Awano, Katsuya,Miyashita, Mitsutomo,Ishizaki, Takayoshi,Kuriyama, Kazuhiko,Sakoe, Yasuhiko,Kudoh, Shinji,Saito, Koji,Kojima, Eisuke

, p. 1519 - 1524 (1997)

A study of the structural optimization of tetrahydroquinoline-6-acetic acid and the development of a novel DMARD with prompt action are detailed. (S)-(+)-8-Chloro-1,2,3,4-tetrahydro-2-trifluoromethyl-6- quinolineacetic acid (IRA-378) exhibits the effect against both acute and chronic inflammations. It also has suppressive effects of bone destruction in adjuvant arthritis and Ca release from bones in vitro.

Cyclic aminophenylacetic acid derivatives, process for preparing the same and immune response modulator having the same as an effective ingredient

-

, (2008/06/13)

The present invention provides novel cyclic aminophenylacetic acid derivatives having modulating action on immune response, their optical isomers, their salts and their preparative processes, and therapeutic agents for autoimmune diseases containing them as effective ingredients, the cyclic aminophenylacetic acid derivatives being represented by a general formula (1) STR1 wherein R and R1 each independently denotes hydrogen atom or lower alkyl group having 1 to 3 carbon atoms, R2 denotes a phenyl group (which may be substituted with 1 to 3 groups of halogen atom, methoxy group or their combinations) or trifluoromethyl group, and X denotes a hydrogen atom, lower alkyl group having 1 to 3 carbon atoms, lower alkoxy group having 1 to 3 carbon atoms, cyano group, thiocyano group, trimethylsilylethinyl group, phenyl group (which may be substituted with halogen atom, methoxy group, methyl group or their combinations), carbamoyl group, carboxyl group, lower alkoxycarbonyl group having 1 to 3 carbon atoms, acetyl group, benzoyl group, nitro group, amino group, lower alkanoylamino group having 1 to 3 carbon atoms, benzoylamino group which may be substituted, phenylsulfonylamino group which may be substituted, lower alkylthio group having 1 to 3 carbon atoms, lower alkylsulfinyl group having 1 to 3 carbon atoms, lower alkylsulfonyl group having 1 to 3 carbon atoms or halogen atom.

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