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196194-97-5

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196194-97-5 Usage

General Description

N-(4-Methoxy-2-Methyl-5-nitrophenyl)acetaMide is a chemical compound with the molecular formula C10H12N2O4. It is a yellow solid, and it is commonly used as an intermediate in the synthesis of pharmaceutical drugs and organic compounds. N-(4-Methoxy-2-Methyl-5-nitrophenyl)acetaMide is known for its analgesic and anti-inflammatory properties, and it has been studied for its potential use in treating various medical conditions. Its structure contains a nitro group, a phenyl group, and an amide group, which give it its unique properties and make it a valuable ingredient in chemical reactions and drug development. Overall, N-(4-Methoxy-2-Methyl-5-nitrophenyl)acetaMide is an important chemical with diverse applications in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 196194-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,1,9 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 196194-97:
(8*1)+(7*9)+(6*6)+(5*1)+(4*9)+(3*4)+(2*9)+(1*7)=185
185 % 10 = 5
So 196194-97-5 is a valid CAS Registry Number.

196194-97-5SDS

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 N-(4-Methoxy-2-methyl-5-nitrophenyl)acetamide

1.2 Other means of identification

Product number -
Other names 2'-Nitro-4'-isopropylacetanilide

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:196194-97-5 SDS

196194-97-5Relevant articles and documents

Substituted quinolinone inhibitor

-

, (2018/09/08)

The invention provides a substituted quinolinone inhibitor and relates to a compound as shown in a formula (II) which is described in the specification or a pharmaceutically acceptable salt, solvate,active metabolite, polymorphic substance, ester, isomer or prodrug thereof, a pharmaceutical composition containing the compound as shown in the formula (II), and application of the compound and the pharmaceutical composition to treatment of diseases related to abnormal TOPK activity.

Double-sided α-helix mimetics

Thompson, Sam,Vallinayagam, Ramakrishnan,Adler, Marc J.,Scott, Richard T.W.,Hamilton, Andrew D.

experimental part, p. 4501 - 4505 (2012/07/17)

The design and synthesis of substituted bis- and tris-benzamides is reported in which the projection of side-chain residues on both sides of an α-helix is reproduced. The scaffold is conformationally constrained by a series of intramolecular hydrogen bonds, allowing for spatial and angular mimicry of the i, i+2, i+4 and i+6 side-chains in the case of the bis-benzamide, and may be extended to higher-order oligomers.

Quinazoline derivatives as VEGF inhibitors

-

, (2008/06/13)

The invention relates to quinazoline derivatives of formula (I) STR1wherein: Z represents --O--, --NH-- or --S--; m is an integer from 1 to 5; R 1 represents hydrogen, hydroxy, halogeno, nitro, trifluorometlyl, cyano, C 1-3 alkyl, C 1-3 alkoxy, C 1-3 alkylthio or NR 5 R 6 (wherein R 5 and R 6, which may be the same or different, each represents hydrogen or C 1-3 alkyl); R 2 represents hydrogen, hydroxy, halogeno, methoxy, amino, or nitro; R 3 represents hydroxy, halogeno, C 1-3 alkyl, C 1-3 alkoxy, C 1-3 alkanoyloxy, trifluoromethyl, cyano, amino or nitro; X 1 represents --O--, --CH 2 --, --S--, --SO--, SO 2 --, --NR 6 --, NR 8 CO--, --CONR 9 --SO 2 NR 10 -- or --NR 11 SO 2 --, (wherein R 7, R 8, R 9, R 10 and R 11 each represents C 1-3 alkyl, C 1-3 alkoxyC 2-3 alkyl); R 4 represents a group which is alkenyl, alkynyl or optionally substituted alkyl, which alkyl group may contain a heteroatom linking group, which alkenyl, alkynyl or alkyl group may carry a terminal optionally substituted 5 or 6 membered saturated carbocylic or heterocyclic group; and salts thereof, processes for their preparation, pharmaceutical compositions containing a compound of formula (I) or a pharmaceutically acceptable salt thereof as active ingredient the compounds of formula (I) and the pharmaceutically acceptable salts thereof inhibit the effects of VEGF, a property of value in the treatment of a number of disease states including cancer and rheumatoid arthritis.

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