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10350-10-4

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  • TIANFUCHEM-10350-10-4--High purity ETHYL 4-HYDROXY-6-METHYL-2-OXO-1,2-DIHYDROPYRIDINE-3-CARBOXYLATE in stock

    Cas No: 10350-10-4

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10350-10-4 Usage

Uses

Ethyl 2,4-Dihydroxy-6-methylnicotinate, is a building block used for various chemical compounds. It is used for the synthesis of analogs of Lucanthone, having antitumor and bactericidal properties.

Check Digit Verification of cas no

The CAS Registry Mumber 10350-10-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,5 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10350-10:
(7*1)+(6*0)+(5*3)+(4*5)+(3*0)+(2*1)+(1*0)=44
44 % 10 = 4
So 10350-10-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO4/c1-3-14-9(13)7-6(11)4-5(2)10-8(7)12/h4H,3H2,1-2H3,(H2,10,11,12)

10350-10-4 Well-known Company Product Price

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  • Aldrich

  • (L510580)  Ethyl 2,4-dihydroxy-6-methylnicotinate  AldrichCPR

  • 10350-10-4

  • L510580-1G

  • 128.70CNY

  • Detail

10350-10-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-hydroxy-6-methyl-2-oxo-1,2-dihydropyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names ETHYL 4-HYDROXY-6-METHYL-2-OXO-1,2-DIHYDROPYRIDINE-3-CARBOXYLATE

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:10350-10-4 SDS

10350-10-4Relevant articles and documents

Process method for producing 3-ethyl formate-4-hydroxy-2-pyridone by utilizing carbon dioxide

-

Paragraph 0018; 0022; 0043-0044; 0053-0054, (2019/08/01)

The invention discloses a process method for producing 3-ethyl formate-4-hydroxy-2-pyridone by utilizing carbon dioxide. The process method comprises the following steps: weighing a 4-hydroxy-6-alkyl-2-pyridone substrate, a catalyst and potassium tert-butoxide to be added into a Schleck bottle, degassing, and continuously introducing 1atm of carbon dioxide; adding a solvent, and reacting in an oilbath; performing after-treatment after the reaction is completed so as to obtain a 3-carboxyl-4-hydroxy-2-pyridone compound 2; carrying out an esterification reaction among the obtained compound 2,(1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride), 2-methylaminopyridine and ethanol; performing column chromatography isolation after the reaction is completed, thereby obtaining the 3-ethyl formate-4-hydroxy-2-pyridone 3. According to the process method disclosed by the invention, the used catalyst is wide in source and low in price; the preparation process is simple, the equipment requirement is low, the raw material is wide in source and low in cost, the toxicity is low, and industrial scale-up production is easily realized.

Thermal Cyclization of 3-Acyl-4-azidopyridines to Isoxazolo[4,3-c]pyridines

Stadlbauer, Wolfgang,Fiala, Werner,Fischer, Michaela,Hojas, Gerhard

, p. 33 - 39 (2007/10/03)

4-Azidopyridines such as 3-acetyl-4-azido-2-pyridones 3 or 4-azido-3-ethoxycarbonylpyridine 7 with reactive ortho-acyl substituents were obtained from the 4-hydroxy-2-pyridones 1, resp. 5 via 4-tosyloxy-2-pyridones 2 or the 2,4-dichloropyridine 6. DSC-ass

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