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3-Quinolinecarboxylicacid,4-amino-2-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75353-49-0

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75353-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75353-49-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,5 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75353-49:
(7*7)+(6*5)+(5*3)+(4*5)+(3*3)+(2*4)+(1*9)=140
140 % 10 = 0
So 75353-49-0 is a valid CAS Registry Number.

75353-49-0SDS

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 4-amino-2-methylquinoline-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Quinolinecarboxylicacid,4-amino-2-methyl

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:75353-49-0 SDS

75353-49-0Downstream Products

75353-49-0Relevant academic research and scientific papers

METHOD OF IMPROVING STABILITY OF SWEET ENHANCER AND COMPOSITION CONTAINING STABILIZED SWEET ENHANCER

-

Paragraph 0284; 0285; 0302; 0303, (2015/09/23)

The present invention includes methods of stabilizing one or more sweet enhancers when they are exposed to a light source as well as liquid compositions containing one or more sweet enhancers and one or more photostabilizers.

Heterocycle-to-heterocycle route to quinoline-4-amines: Reductive heterocyclization of 3-(2-nitrophenyl)isoxazoles

Coffman, Keith C.,Duong, Vy,Bagdasarian, Alex L.,Fettinger, James C.,Haddadin, Makhluf J.,Kurth, Mark J.

, p. 7651 - 7657 (2015/04/22)

A variety of quinoline-4-amines were synthesized from substituted 3-(2-nitrophenyl)isoxazoles utilizing Zn0 or Fe0 dust and HOAc using a reductive heterocyclization process. The starting isoxazoles were synthesized from readily available starting materials. A brief survey of functional groups tolerated in this reductive heterocyclization was performed and several 10-amino-3,4-dihydrobenzo[b][1,6]naphthyridin-1(2H)-one and 9-amino-3,4-dihydroacridin-1(2H)-one examples were synthesized.

METHOD OF IMPROVING STABILITY OF SWEET ENHANCER AND COMPOSITION CONTAINING STABILIZED SWEET ENHANCER

-

, (2012/03/08)

The present invention includes methods of stabilizing one or more sweet enhancers when they are exposed to a light source as well as liquid compositions containing one or more sweet enhancers and one or more photostabilizers.

SWEET FLAVOR MODIFIER

-

, (2011/10/13)

The present invention includes compounds having structural formula (I), or pharmaceutically acceptable salts, solvate, and/or ester thereof. These compounds are useful as sweet flavor modifiers. The present invention also includes compositions comprising the present compounds and methods of enhancing the sweet taste of ingestible compositions. Furthermore, the present invention provides methods for preparing the compounds.

Synthesis of 4-Quinolone Derivatives

Jensen, Soeren,Torssell, Kurt B. G.

, p. 53 - 56 (2007/10/02)

Routes to 4-amino-2-alkyl substituted quinoline-3-carboxylic acids and 3-acyl-2-phenyl and 3-acyl-2-alkyl substituted 4-quinolones have been devised by application of isoxazole chemistry and Heck-Stille couplings.

Sur les orthoamino formyl quinoleines, nouveaux synthons heterocycliques

Godard, Alain,Queguiner, Guy

, p. 465 - 473 (2007/10/02)

Les quatre orthoamino formyl quinoleines substituees sur le cycle pyridinique ont ete synthetisees par oxydation des amino hydroxymethyl quinoleines correspondantes.Parmi toutes les methodes envisagees, seule cette derniere a permis la preparation de l'amino-3 formyl-2 quinoleine, compose relativement peu stable.Ces nouveaux composes bifonctionnels derives de la qunoleine constituent des synthons particulierement interessants pour l'elaboration de certains heterocycles.

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