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10349-57-2

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10349-57-2 Usage

Chemical Properties

beige to brown crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 10349-57-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,4 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10349-57:
(7*1)+(6*0)+(5*3)+(4*4)+(3*9)+(2*5)+(1*7)=82
82 % 10 = 2
So 10349-57-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H7NO2/c12-10(13)8-3-4-9-7(6-8)2-1-5-11-9/h1-6H,(H,12,13)/p-1

10349-57-2 Well-known Company Product Price

  • Brand
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  • Alfa Aesar

  • (A18223)  Quinoline-6-carboxylic acid, 98%   

  • 10349-57-2

  • 1g

  • 1028.0CNY

  • Detail
  • Alfa Aesar

  • (A18223)  Quinoline-6-carboxylic acid, 98%   

  • 10349-57-2

  • 5g

  • 4094.0CNY

  • Detail
  • Alfa Aesar

  • (A18223)  Quinoline-6-carboxylic acid, 98%   

  • 10349-57-2

  • 25g

  • 7413.0CNY

  • Detail

10349-57-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Quinolinecarboxylic acid

1.2 Other means of identification

Product number -
Other names Quinoline-6-Carboxylic Acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10349-57-2 SDS

10349-57-2Relevant articles and documents

SYNTHESIS AND PHARMACOLOGICAL PROPERTIES OF THE ALKALOID KOMAROVININE AND ITS TETRAHYDRO DERIVATIVE

Tulyaganov, T. S.,Ibragimov, A. A.,Yunusov, S. Yu.,Vakhabov, A. A.,Aminov, S. D.

, p. 182 - 184 (1987)

-

Remarkable effect of nitrogen dioxide for N-hydroxyphthalimide-catalyzed aerobic oxidation of methylquinolines

Sakaguchi, Satoshi,Shibamoto, Akihiro,Ishii, Yasutaka

, p. 180 - 181 (2002)

Aerobic oxidation of methylquinolines was successfully achieved by the use of N-hydroxyphthalimide/Co(OAc)2/Mn(OAc)2 as catalyst in the presence of a small amount of nitrogen dioxide as an initiator.

Visible-light-mediated organoboron-catalysed metal-free dehydrogenation of N-heterocycles using molecular oxygen

Wei, Lanfeng,Wei, Yu,Xu, Liang,Zhang, Jinli

supporting information, p. 4446 - 4450 (2021/06/30)

The surge of photocatalytic transformation not only provides unprecedented synthetic methods, but also triggers the enthusiasm for more sustainable photocatalysts. On the other hand, oxygen is an ideal oxidant in terms of atom economy and environmental friendliness. However, the poor reactivity of oxygen at the ground state makes its utilization challenging. Herein, a visible-light-induced oxidative dehydrogenative process is disclosed, which uses an organoboron compound as the photocatalyst and molecular oxygen as the sole oxidant.Viathis approach, an array of N-heterocycles have been accessed under metal-free mild conditions, in good to excellent yields.

Method for preparing aromatic carboxylic acid compound

-

Paragraph 0085-0086; 0136-0139; 0176, (2020/02/14)

The invention discloses a method for preparing an aromatic carboxylic acid compound. The method comprises the following steps: 1) heating carbon dioxide and hydrosilane in the presence of a copper catalyst in a reaction medium A; and 2) adding a reaction medium B, aryl halide, a palladium catalyst and a base to the reaction mixture in the step 1), sealing the reaction system, and performing a heating reaction. The method has the advantages that raw materials are simple and easy to obtain, the raw materials are cheap and stable, the catalyst is common, easy to obtain and stable, the reaction conditionsaremild, the aftertreatment is simple, the yield is high, and the like.

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