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184098-19-9

3-(2-methyl-1h-imidazol-1-yl)aniline is a chemical compound characterized by its molecular formula C10H12N2. It is a white to off-white solid that serves as a crucial building block in the synthesis of various pharmaceuticals and organic compounds. As a derivative of aniline, it features both an imidazole and aniline group in its structure, which endows it with unique chemical properties and makes it a versatile precursor for the synthesis of a range of heterocyclic compounds. 3-(2-methyl-1h-imidazol-1-yl)aniline is an important chemical intermediate with a wide array of applications in the pharmaceutical and chemical industries.

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  • 184098-19-9 Structure

  • Basic information

    1. Product Name: 3-(2-methyl-1h-imidazol-1-yl)aniline
    2. Synonyms: 3-(2-methyl-1h-imidazol-1-yl)aniline;3-(2-Methyl-1H-imidazol-1-yl)aniline 97%
    3. CAS NO:184098-19-9
    4. Molecular Formula: C10H11N3
    5. Molecular Weight: 173.21444
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 184098-19-9.mol

  • Chemical Properties

    1. Melting Point: 119.5 °C
    2. Boiling Point: 395 °C at 760 mmHg
    3. Flash Point: 192.7 °C
    4. Appearance: /
    5. Density: 1.17 g/cm3
    6. Vapor Pressure: 1.9E-06mmHg at 25°C
    7. Refractive Index: 1.624
    8. Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-(2-methyl-1h-imidazol-1-yl)aniline(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(2-methyl-1h-imidazol-1-yl)aniline(184098-19-9)
    12. EPA Substance Registry System: 3-(2-methyl-1h-imidazol-1-yl)aniline(184098-19-9)

  • Safety Data

    1. Hazard Codes:  Harmful:;
    2. Statements: 41
    3. Safety Statements: 26-39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 184098-19-9(Hazardous Substances Data)

184098-19-9 Usage

Uses

Used in Pharmaceutical Industry:
3-(2-methyl-1h-imidazol-1-yl)aniline is used as a key intermediate in the synthesis of biologically active compounds for treating various medical conditions. Its presence in the structure of these compounds contributes to their therapeutic effects.
Used in Organic Synthesis:
3-(2-methyl-1h-imidazol-1-yl)aniline is used as a precursor in the synthesis of heterocyclic compounds, which are essential in the development of new pharmaceuticals and organic materials.
Used in Chemical Industry:
3-(2-methyl-1h-imidazol-1-yl)aniline is utilized as a chemical intermediate in the production of various organic compounds, contributing to the advancement of chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 184098-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,0,9 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 184098-19:
(8*1)+(7*8)+(6*4)+(5*0)+(4*9)+(3*8)+(2*1)+(1*9)=159
159 % 10 = 9
So 184098-19-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3/c1-8-12-5-6-13(8)10-4-2-3-9(11)7-10/h2-7H,11H2,1H3

184098-19-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-methylimidazol-1-yl)aniline

1.2 Other means of identification

Product number -
Other names -

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:184098-19-9 SDS

184098-19-9Relevant articles and documents

EFFICIENT LIGAND-MEDIATED ULLMANN COUPLING OF ANILINES AND AZOLES

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Page 32, (2008/06/13)

The present invention provides of method of preparing phenyl-substituted azoles. This method uses an efficient ligand-accelerated Ullmann coupling reaction of anilines with azoles. The coupling products are useful for preparing factor Xa inhibitors.

Efficient ligand-mediated ullmann coupling of anilnies and azoles

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, (2008/06/13)

The present invention provides of method of preparing phenyl-substituted azoles. This method uses an efficient ligand-accelerated Ullmann coupling reaction of anilines with azoles. The coupling products are useful for preparing factor Xa inhibitors.

Novel imidazole compound and anti-depressing agent containing the same

-

, (2008/06/13)

An imidazole compound of the formula: STR1 wherein R1 is lower alkyl, R2 is hydrogen or lower alkyl, and R3, R4 and R5 are hydrogen, lower alkyl, trifluoromethyl, amino, mono- or di-lower alkylamino,

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