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32896-90-5

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32896-90-5 Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 21, p. 874, 1978 DOI: 10.1021/jm00207a007Tetrahedron Letters, 12, p. 2211, 1971 DOI: 10.1016/S0040-4039(01)96822-4

Check Digit Verification of cas no

The CAS Registry Mumber 32896-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,8,9 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 32896-90:
(7*3)+(6*2)+(5*8)+(4*9)+(3*6)+(2*9)+(1*0)=145
145 % 10 = 5
So 32896-90-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O3/c1-7-4-5(8(10)11)2-3-6(7)9/h2-4H,1H3

32896-90-5SDS

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 1-methyl-5-nitropyridin-2-one

1.2 Other means of identification

Product number -
Other names 5-nitro-N-methylpyridone

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:32896-90-5 SDS

32896-90-5Relevant articles and documents

Hilbert-Johnson reaction under high pressure: A facile preparation of 2-pyridones

Matsumoto, Kiyoshi,Ikemi, Yukio,Suda, Machiko,Iida, Hirokazu,Hamana, Hiroshi

, p. 187 - 190 (2007)

For the first time, a facile synthesis of 2-pyridones utilizing a classical Hilbert-Johnson reaction of 2-methoxypyridines with haloalkanes under high pressure has been achieved. The reactions were sensitive to steric hindrance of haloalkanes.

NITRATION OF AROMATIC HETEROCYCLES WITH PALLADIUM(II) ACETATE AND SODIUM NITRITE.

Itahara,Ebihara,Kawasaki

, p. 2171 - 2172 (2007/10/02)

Treatments of 1,3-dimethyluracil, 1-methyl-2-pyridone, and thiophene with palladium(II) acetate and sodium nitrite gave the corresponding nitro-substituted products.

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