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2-Pyridinamine,6-butyl-(9CI) is a chemical compound with the molecular formula C11H16N2. It is a derivative of pyridine, featuring a butyl group attached to the sixth carbon atom of the pyridine ring. This versatile chemical is known for its potential biological and pharmacological activities, including antifungal and antibacterial properties, and is widely used in organic synthesis for the preparation of pharmaceuticals, agrochemicals, and other fine chemicals.

95337-74-9

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95337-74-9 Usage

Uses

Used in Organic Synthesis:
2-Pyridinamine,6-butyl-(9CI) is used as a building block in organic synthesis for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and functional groups make it a valuable component in the development of new compounds with specific therapeutic or chemical properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Pyridinamine,6-butyl-(9CI) is used as an intermediate in the synthesis of drugs with potential therapeutic applications. Its presence in the molecular structure of these drugs can contribute to their biological activity and pharmacological properties, making it an essential component in drug discovery and development.
Used in Agrochemical Industry:
2-Pyridinamine,6-butyl-(9CI) is also utilized in the agrochemical industry for the synthesis of compounds with pesticidal or herbicidal properties. Its incorporation into these agrochemicals can enhance their effectiveness in controlling pests and weeds, thereby contributing to increased crop yields and agricultural productivity.
Used in Drug Discovery:
2-Pyridinamine,6-butyl-(9CI) has been studied for its potential biological and pharmacological activities, including its antifungal and antibacterial properties. Researchers are exploring its use in drug discovery to develop new therapeutic agents that can combat various infections and diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 95337-74-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,3 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 95337-74:
(7*9)+(6*5)+(5*3)+(4*3)+(3*7)+(2*7)+(1*4)=159
159 % 10 = 9
So 95337-74-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N2/c1-2-3-5-8-6-4-7-9(10)11-8/h4,6-7H,2-3,5H2,1H3,(H2,10,11)

95337-74-9SDS

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 6-butylpyridin-2-amine

1.2 Other means of identification

Product number -
Other names 6-butyl-2-pyridinamine

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:95337-74-9 SDS

95337-74-9Relevant academic research and scientific papers

Design and synthesis of substituted N-(1,3-diphenyl-1H-pyrazol-5-yl) benzamides as positive allosteric modulators of the metabotropic glutamate receptor subtype 5

Zou, Mu-Fa,Cao, Jianjing,Rodriguez, Alice L.,Jeffrey Conn,Newman, Amy Hauck

, p. 2650 - 2654 (2011/06/20)

Based on SAR in the alkyne class of mGlu5 receptor negative allosteric modulators and a set of amide-based positive allosteric modulators, optimized substitution of the aryl bring was used to create substituted N-(1,3-diphenyl-1H-pyrazol-5-yl)benzamides.

Bisaryl-sulfonamides

-

Page/Page column 30, (2008/06/13)

Compounds, compositions and methods are provided that are useful in the treatment or prevention of a condition or disorder mediated by PPARγ or PPARδ. In particular, the compounds of the invention modulate the function of PPARγ or PPARδ. The subject methods are particularly useful in the treatment and/or prevention of diabetes, obesity, hypercholesterolemia, rheumatoid arthritis and atherosclerosis.

Protection of Primary Amines as N-Substituted 2,5-Dimethylpyrroles

Bruekelman, Stephen P.,Leach, (Miss) Susan E.,Meakins, G. Denis,Tirel, Malcolm D.

, p. 2801 - 2807 (2007/10/02)

Protection of primary amine group is achieved by incorporating it into an N-substituted 2,5-dimethylpyrrole system.The method affords protection against strong bases and nucleophiles, heating with concentrated alkali, standard mineral acid work-up conditions, and various other reagents.Phenyl-, pyridil-, thiazolyl-, and alkyl-amines have been studied.All give trisubstituted pyrroles in high yield (>80percent) by reaction with hexane-2,5-dione.The pyrroles from the first three types are stable to storage; even the N-alkyl compounds can be used without difficulty.Regeneration of the amine group, by treatment with hydrxylamine hydrochloride, is efficient (80percent yield) with the phenyl, pyridyl, and alkyl compounds but less satisfactory (60 - 65percent generally but down to 25percent in two cases) with the thiazolyl derivatives.

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