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CAS

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120456-35-1

1-AMINO-4,6-DIMETHYL-5-(METHYLTHIO)-2-OXO-1,2-DIHYDROPYRIDINE-3-CARBONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1-AMINO-4,6-DIMETHYL-5-(METHYLTHIO)-2-OXO-1,2-DIHYDROPYRIDINE-3-CARBONITRILE

    Cas No: 120456-35-1

  • USD $ 1.9-2.9 / Gram

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  • 120456-35-1 Structure

  • Basic information

    1. Product Name: 1-AMINO-4,6-DIMETHYL-5-(METHYLTHIO)-2-OXO-1,2-DIHYDROPYRIDINE-3-CARBONITRILE
    2. Synonyms: 1-amino-4,6-dimethyl-5-(methylthio)-2-oxo-1,2-dihydropyridine-3-carbonitrile; 1-amino-4,6-dimethyl-5-(methylsulfanyl)-2-oxo-1,2-dihydropyridine-3-carbonitrile
    3. CAS NO:120456-35-1
    4. Molecular Formula: C9H11N3OS
    5. Molecular Weight: 209.27
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 120456-35-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 282.6°Cat760mmHg
    3. Flash Point: 124.7°C
    4. Appearance: /
    5. Density: 1.3g/cm3
    6. Vapor Pressure: 0.00332mmHg at 25°C
    7. Refractive Index: 1.618
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-AMINO-4,6-DIMETHYL-5-(METHYLTHIO)-2-OXO-1,2-DIHYDROPYRIDINE-3-CARBONITRILE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-AMINO-4,6-DIMETHYL-5-(METHYLTHIO)-2-OXO-1,2-DIHYDROPYRIDINE-3-CARBONITRILE(120456-35-1)
    12. EPA Substance Registry System: 1-AMINO-4,6-DIMETHYL-5-(METHYLTHIO)-2-OXO-1,2-DIHYDROPYRIDINE-3-CARBONITRILE(120456-35-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 120456-35-1(Hazardous Substances Data)

120456-35-1 Usage

Chemical Class

Dihydropyridine derivative

Explanation

The compound belongs to the class of dihydropyridines, which are characterized by a six-membered ring with two hydrogen atoms in a specific arrangement.

Explanation

The compound has a complex molecular structure due to the presence of multiple functional groups and a fused ring system.

Explanation

The compound contains an amino group (-NH2), two methyl groups (-CH3), a thiomethyl group (-SCH3), a nitrile group (-CN), and a ketone group (C=O).

Explanation

The compound's versatile chemical structure with multiple functional groups makes it a candidate for potential applications in the fields of biology and pharmaceuticals.

Explanation

The presence of multiple functional groups and a fused ring system makes the compound an interesting target for research and development in the fields of organic chemistry and drug discovery.

Explanation

The compound features a pyridine ring (a six-membered nitrogen-containing ring) fused with another six-membered ring, contributing to its complex structure.

Explanation

The material provided does not mention any information about the stereochemistry (3D arrangement) of the compound.

Explanation

The material provided does not mention any information about the solubility of the compound in different solvents.

Explanation

The material provided does not mention any information about the stability of the compound under various conditions.

Explanation

The material provided does not mention any information about the reactivity of the compound with other chemicals or under different conditions.

Molecular Structure

Complex

Functional Groups

Amino, methyl, thiomethyl, nitrile, and ketone

Potential Applications

Biological and pharmaceutical

Research and Development

Organic chemistry and drug discovery

Fused Ring System

Pyridine ring fused with a six-membered ring

Stereochemistry

Not specified in the material

Solubility

Not specified in the material

Stability

Not specified in the material

Reactivity

Not specified in the material

Check Digit Verification of cas no

The CAS Registry Mumber 120456-35-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,4,5 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 120456-35:
(8*1)+(7*2)+(6*0)+(5*4)+(4*5)+(3*6)+(2*3)+(1*5)=91
91 % 10 = 1
So 120456-35-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H11N3OS/c1-5-7(4-10)9(13)12(11)6(2)8(5)14-3/h11H2,1-3H3

120456-35-1SDS

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 1-amino-4,6-dimethyl-5-methylsulfanyl-2-oxopyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 1-Amino-4,6-dimethyl-5-methylthio-2-oxo-1,2-dihydropyridin-3-carbonitril

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:120456-35-1 SDS

120456-35-1Upstream product

120456-35-1Relevant articles and documents

Ringtransformation of Ethyl 2-Amino-thiophene-3-carboxylates: Derivatives of Pyridones and Pyridazinones

Gewald, Karl,Gruner, Margit,Hain, Ute,Sueptitz, Gabriele

, p. 985 - 992 (2007/10/02)

Whereas treatment of the ethyl 5-acetyl-2-amino-4-methyl-thiophene-3-carboxylate (1) with potassium hydroxide yields the 2-hydroxy-thiophene-3-carbonitrile 4 its hydrazone 2 is converted into the 1-amino-5-mercapto-2-pyridone derivative 6.The transformation of the 2-amino-5-phenylazo-thiophene derivative 9 by potassium hydroxide yields the substituted 3-mercapto-pyridazin-6(1H)one 10, with sodium ethoxide the 5-phenylhydrazone-2-oxo-thiolen-3-carbonitrile 11 is formed.From 6 the 5-mercapto-2-pyridone derivatives 7d, e can be obtained. - Keywords: 2-Aminothiophene-3-carboxylic acid derivatives; 1-Amino-2-pyridone; 1,2-Dihydro-2-oxo-pyridine-5-thioles; Pyridazin-6(1H)-one

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