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183670-12-4

2-(2-nitrophenyl)-quinoline-4-carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 183670-12-4 Structure

  • Basic information

    1. Product Name: 2-(2-nitrophenyl)-quinoline-4-carboxylic acid
    2. Synonyms: 2-(2-nitrophenyl)-quinoline-4-carboxylic acid
    3. CAS NO:183670-12-4
    4. Molecular Formula:
    5. Molecular Weight: 294.266
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 183670-12-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(2-nitrophenyl)-quinoline-4-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-nitrophenyl)-quinoline-4-carboxylic acid(183670-12-4)
    11. EPA Substance Registry System: 2-(2-nitrophenyl)-quinoline-4-carboxylic acid(183670-12-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 183670-12-4(Hazardous Substances Data)

183670-12-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183670-12-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,6,7 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 183670-12:
(8*1)+(7*8)+(6*3)+(5*6)+(4*7)+(3*0)+(2*1)+(1*2)=144
144 % 10 = 4
So 183670-12-4 is a valid CAS Registry Number.

183670-12-4Downstream Products

183670-12-4Relevant articles and documents

Design, synthesis and antibacterial evaluation of some new 2-phenyl-quinoline-4-carboxylic acid derivatives

Wang, Xiaoqin,Xie, Xiaoyang,Cai, Yuanhong,Yang, Xiaolan,Li, Jiayu,Li, Yinghan,Chen, Wenna,He, Minghua

, (2016)

A series of new 2-phenyl-quinoline-4-carboxylic acid derivatives was synthesized starting from aniline, 2-nitrobenzaldehyde, pyruvic acid followed by Doebner reaction, amidation, reduction, acylation and amination. All of the newly-synthesized compounds w

STAT3 INHIBITOR CONTAINING QUINOLINECARBOXAMIDE DERIVATIVE AS ACTIVE INGREDIENT

-

Page/Page column 62, (2011/06/24)

The present invention provides a STAT3 inhibitor containing as an active ingredient, a quinolinecarboxamide derivative represented by the formula (I) (in the formula, W represents a bond or an alkylene chain; X represents O, S, or NR34; and Rs

Microwave-assisted Doebner synthesis of 2-phenylquinoline-4-carboxylic acids and their antiparasitic activities

Muscia, Gisela C.,Carnevale, Juan P.,Bollini, Mariela,Asis, Silvia E.

, p. 611 - 614 (2008/09/19)

(Chemical Equation Presented) A series of twelve substituted 2-phenylquinoline-4-carboxylic acids analogous to antimalarial and antileishmanial natural products was developed via the Doebner reaction employing microwave irradiation (MW). The products were obtained in moderate yields in 0.5-3 minutes and nine of them were evaluated in vitro against the parasites responsible for malaria, leishmaniasis and trypanosomiasis diseases (WHO, Switzerland). Four compounds exhibited activity against Trypanosoma cruzi and another two resulted active against Plasmodium falciparum and Leishmania infantum, respectively.

Separation of 2(3),9(10),16(17),23(24)-tetrasubstituted phthalocyanines with newly developed HPLC phases

Sommerauer, Michael,Rager, Christine,Hanack, Michael

, p. 10085 - 10093 (2007/10/03)

The synthesis of 2(3),9(10),16(17),23(24)-tetrasubstituted phthalocyanines from 1,2-dicyano-4-alkoxybenzenes or the corresponding isoindolines is reported. In each case, four isomers with D(2h), C(4h), C(2v), and C(s) symmetry are obtained in the statisti

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