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149281-42-5

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149281-42-5 Usage

General Description

6-Chloro-N-methoxy-N-methyl-nicotinamide is a chemical compound with the molecular formula C9H10ClN2O2. It is a derivative of nicotinamide and contains a chlorine atom, a methoxy group, and a methyl group attached to the nicotinamide ring. 6-CHLORO-N-METHOXY-N-METHYL-NICOTINAMIDE is used in chemical research and has potential applications in the pharmaceutical industry. It may be used in the synthesis of new drugs or as a starting material for the development of new chemical compounds with biological activity. Additionally, 6-Chloro-N-methoxy-N-methyl-nicotinamide may have properties that make it useful for studying biological processes and mechanisms in the body.

Check Digit Verification of cas no

The CAS Registry Mumber 149281-42-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,2,8 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 149281-42:
(8*1)+(7*4)+(6*9)+(5*2)+(4*8)+(3*1)+(2*4)+(1*2)=145
145 % 10 = 5
So 149281-42-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H9ClN2O2/c1-11(13-2)8(12)6-3-4-7(9)10-5-6/h3-5H,1-2H3

149281-42-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-N-methoxy-N-methylpyridine-3-carboxamide

1.2 Other means of identification

Product number -
Other names 6-chloro-N-methoxy-N-methylpyridin-3-carboxamide

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:149281-42-5 SDS

149281-42-5Relevant articles and documents

Direct synthesis of β-aminoketones from amides via novel sequential nucleophilic substitution/Michael reaction

Gomtsyan, Arthur

, p. 11 - 13 (2000)

(formula presented) The synthesis of β-aminoketones from amides can be achieved in a process consisting of sequential nucleophilic substitution at the carbonyl group by vinylmagnesium bromide followed by Michael reaction after quench of the first reaction

PYRIDIN-3-YL ACETIC ACID DERIVATIVES AS INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION

-

Page/Page column 130; 131, (2018/08/04)

Disclosed are compounds of Formula I, including pharmaceutically acceptable salts, pharmaceutical compositions comprising the compounds, methods for making the compounds and their use in inhibiting HIV integrase and treating those infected with HIV or AIDS. (I)

Discovery of novel 2-[(4-hydroxy-6-oxo-2,3-dihydro-1H-pyridine-5-carbonyl)amino]acetic acid derivatives as HIF prolyl hydroxylase inhibitors for treatment of renal anemia

Hamada, Makoto,Takayama, Tetsuo,Shibata, Tsuyoshi,Hiratate, Akira,Takahashi, Masato,Yashiro, Miyoko,Takayama, Noriko,Okumura-Kitajima, Lisa,Koretsune, Hiroko,Kajiyama, Hiromitsu,Naruse, Takumi,Kato, Sota,Takano, Hiroki,Kakinuma, Hiroyuki

supporting information, p. 1725 - 1730 (2018/04/30)

Prolyl hydroxylase domain-containing protein (PHD) inhibitors are useful as orally administered agents for the treatment of renal anemia. Based on the common structures of known PHD inhibitors, we found novel PHD inhibitor 1 with a 2-[(4-hydroxy-6-oxo-2,3

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