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31557-75-2

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31557-75-2 Usage

General Description

1-(5-Nitropyridin-2-yl)ethanone is a chemical compound with the molecular formula C7H6N2O3. It is a yellow solid that is soluble in various organic solvents. 1-(5-Nitropyridin-2-yl)ethanone is commonly used in the synthesis of various pharmaceuticals and agrochemicals. It also has potential applications in the field of materials science, particularly in the development of organic semiconducting materials. The presence of a nitro group in the molecule gives it significant chemical reactivity, making it useful in a variety of synthetic processes. Overall, 1-(5-Nitropyridin-2-yl)ethanone is a versatile chemical compound with diverse applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 31557-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,5,5 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 31557-75:
(7*3)+(6*1)+(5*5)+(4*5)+(3*7)+(2*7)+(1*5)=112
112 % 10 = 2
So 31557-75-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O3/c1-5(10)7-3-2-6(4-8-7)9(11)12/h2-4H,1H3

31557-75-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(5-Nitropyridin-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(5-nitro-2-pyridinyl)ethanone

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:31557-75-2 SDS

31557-75-2Downstream Products

31557-75-2Relevant articles and documents

Nitropyridines: X.* Palladium-catalyzed cross-coupling of 2-bromo-5-nitropyridine with terminal acetylenes

Sagitullina,Vorontsova,Garkushenko,Poendaev,Sagitullin

experimental part, p. 1830 - 1834 (2011/04/15)

Substituted 5-nitro-2-ethynylpyridines were synthesized by the Sonogashira reaction of 2-bromo-5-5-nitropyridine with terminal acetylenes. Desilylation, oxidative decarbonylation, and the retro-Favorskii reaction of the cross-coupling products of 2-bromo-5-nitropyridine with trimethylsilylacetylene, prop-2-ynyl alcohol, and 2-methylbut-3-yn-2-ol, respectively, gave 2-ethynyl-5-nitropyridine. The hydration of 2-ethynyl-5-nitropyridine and 5-nitro-2-(phenylethynyl)pyridine according to Kucherov afforded 2-acetyl-5-nitropyridine and 5-nitro-2-phenacylpyridine, respectively. Pleiades Publishing, Ltd., 2010.

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