• Product NameQuinaldic acid
  • CasNo. 93-10-7
  • MFC10H7NO2
  • MW173.171
  • Purity
  • Appearancelight brown needle-like crystalline powder
  • Packing
  • Contact usInquiry

Product Details

CasNo: 93-10-7

MF: C10H7NO2

Appearance: light brown needle-like crystalline powder

Manufacturer supply top purity Quinaldic acid 93-10-7 with ISO standards

  • Molecular Formula:C10H7NO2
  • Molecular Weight:173.171
  • Appearance/Colour:light brown needle-like crystalline powder 
  • Vapor Pressure:1.85E-05mmHg at 25°C 
  • Melting Point:156-158 °C(lit.) 
  • Refractive Index:1.5200 (estimate) 
  • Boiling Point:348.741 °C at 760 mmHg 
  • PKA:1.20±0.30(Predicted) 
  • Flash Point:164.713 °C 
  • PSA:50.19000 
  • Density:1.339 g/cm3 
  • LogP:1.93300 

Quinaldic acid(Cas 93-10-7) Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 68, p. 1840, 1946 DOI: 10.1021/ja01213a045

Purification Methods

Crystallise quinaldic acid from *C6H6 or AcOH. It is used for the estimation of many metals. The methyl ester has m 86-87o (from hexane) and pK25 1.76. [Chauduri et al. Frez Z Anal Chem 281 361 1976, Beilstein 22 H 71, 22 II 55, 22 III/IV 1149, 22/3 V 183.]

Definition

ChEBI: A quinolinemonocarboxylic acid having the carboxy group at the 2-position.

General Description

Quinaldic acid is also referred as quinoline-2-carboxylic acid. Microwave-assisted preparation of substituted anilides of quinaldic acid has been reported. It inhibits the oxidation of pyruvate, α-ketoglutarate, glutamate and citrate in rat liver mitochondria. Quinaldic acid is a metabolite of tryptophan degradation and inhibits the gluconeogenesis in perfused livers.

InChI:InChI=1/C10H7NO2/c12-10(13)9-6-5-7-3-1-2-4-8(7)11-9/h1-6H,(H,12,13)/p-1

93-10-7 Relevant articles

Oxidation of Primary Alcohols and Aldehydes to Carboxylic Acids via Hydrogen Atom Transfer

Tan, Wen-Yun,Lu, Yi,Zhao, Jing-Feng,Chen, Wen,Zhang, Hongbin

supporting information, p. 6648 - 6653 (2021/09/08)

The oxidation of primary alcohols and al...

Design, synthesis and biological evaluation of novel thiohydantoin derivatives as potent androgen receptor antagonists for the treatment of prostate cancer

Wang, Ao,Wang, Yawan,Meng, Xin,Yang, Yushe

, (2021/01/07)

Prostate cancer (PC) is the most common ...

Repurposing an Aldolase for the Chemoenzymatic Synthesis of Substituted Quinolines

Fansher, Douglas J.,Granger, Richard,Kaur, Satinderpal,Palmer, David R. J.

, p. 6939 - 6943 (2021/06/28)

Quinoline derivatives are important natu...

Nickel-Catalyzed Conversion of Amides to Carboxylic Acids

Bulger, Ana S.,Garg, Neil K.,Knapp, Rachel R.

supporting information, (2020/04/02)

We report the conversion of amides to ca...

93-10-7 Process route

quinoline 2-carbaldehyde
5470-96-2

quinoline 2-carbaldehyde

quinolin-2-ylmethanol
1780-17-2

quinolin-2-ylmethanol

quinoline-2-carboxylic acid
93-10-7,1199266-78-8

quinoline-2-carboxylic acid

Conditions
Conditions Yield
With potassium hydroxide;
1-benzoyl-1,2-dihydro-quinoline-2-carbonitrile
13721-17-0

1-benzoyl-1,2-dihydro-quinoline-2-carbonitrile

quinoline-2-carboxylic acid
93-10-7,1199266-78-8

quinoline-2-carboxylic acid

quinoline-2-carboxamide
5382-42-3

quinoline-2-carboxamide

benzaldehyde
100-52-7

benzaldehyde

Conditions
Conditions Yield
With formic acid; at 20 ℃; for 20h;
98%
82%
1%

93-10-7 Upstream products

  • 830-60-4
    830-60-4

    2H-quinoline-1,2-dicarbonitrile

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    quinoline

  • 74-90-8
    74-90-8

    hydrogen cyanide

  • 91-63-4
    91-63-4

    2-methylquinoline

93-10-7 Downstream products

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    30836-61-4

    1,1-diphenyl-1-(2-quinolyl)methanol

  • 119-91-5
    119-91-5

    2,2'-biquinoline

  • 27104-55-8
    27104-55-8

    α-phenyl-2-quinolinemethanol

  • 16576-27-5
    16576-27-5

    (4-methoxyphenyl)(quinoline-2-yl)methanone

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