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CAS

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53663-37-9

3-(dimethoxymethyl)aniline is a chemical compound with the molecular formula C9H13NO2, belonging to the class of aniline derivatives. It features two methoxy groups and a methyl group attached to the carbon atoms, which contribute to its unique chemical properties. This pale yellow to brown liquid, characterized by a strong odor, is recognized for its role as an intermediate in the synthesis of a variety of organic compounds, including pharmaceuticals, dyes, and polymers. Due to its moderate toxicity and potential to irritate skin and eyes, it requires careful handling and storage in a cool, dry environment away from direct sunlight and heat sources.

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  • 53663-37-9 Structure

  • Basic information

    1. Product Name: 3-(dimethoxymethyl)aniline
    2. Synonyms: 3-(Dimethoxymethyl)aniline; benzenamine, 3-(dimethoxymethyl)-
    3. CAS NO:53663-37-9
    4. Molecular Formula: C9H13NO2
    5. Molecular Weight: 167.205
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 53663-37-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 243°C at 760 mmHg
    3. Flash Point: 108.3°C
    4. Appearance: N/A
    5. Density: 1.082g/cm3
    6. Vapor Pressure: 0.033mmHg at 25°C
    7. Refractive Index: 1.535
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-(dimethoxymethyl)aniline(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(dimethoxymethyl)aniline(53663-37-9)
    12. EPA Substance Registry System: 3-(dimethoxymethyl)aniline(53663-37-9)

  • 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: 53663-37-9(Hazardous Substances Data)

53663-37-9 Usage

Uses

Used in Pharmaceutical Industry:
3-(dimethoxymethyl)aniline serves as a crucial intermediate in the synthesis of pharmaceuticals, facilitating the creation of various medicinal compounds. Its unique structure allows for the development of drugs with specific therapeutic properties, contributing to the advancement of healthcare solutions.
Used in Dye Industry:
In the dye industry, 3-(dimethoxymethyl)aniline is utilized as a building block for the production of dyes. Its chemical structure enables the creation of dyes with distinct color characteristics, enhancing the range of color options available for various applications, including textiles and printing.
Used in Polymer Industry:
3-(dimethoxymethyl)aniline plays a significant role in the polymer industry, where it is employed in the synthesis of polymers with specific properties. Its incorporation into polymer structures can lead to materials with tailored characteristics, such as improved strength, flexibility, or resistance to environmental factors, broadening the scope of polymer applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 53663-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,6 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53663-37:
(7*5)+(6*3)+(5*6)+(4*6)+(3*3)+(2*3)+(1*7)=129
129 % 10 = 9
So 53663-37-9 is a valid CAS Registry Number.

53663-37-9SDS

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 3-(dimethoxymethyl)aniline

1.2 Other means of identification

Product number -
Other names m-aminobenzaldehyde dimethylacetal

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:53663-37-9 SDS

53663-37-9Relevant articles and documents

Conformational analogues of Oxamflatin as histone deacetylase inhibitors

Dear, Anthony E.,Liu, Hong B.,Mayes, Penelope A.,Perlmutter, Patrick

, p. 3778 - 3784 (2008/09/18)

Conformational analogues of the hydroxamic acid Oxamflatin 1 - compounds 3a, 3b and 4 - have been synthesised to enable evaluation of the impact of varying the linking section on histone deacetylase inhibition. Preliminary testing indicates treatment of l

Synthesis and structural analysis of 1,4-bis[n-(N,N-di-methylamino)phenyl]buta-1,3-diynes and charge-transfer complexes with TCNE

Rodriguez, J. Gonzalo,Lafuente, Antonio,Martin-Villamil, Rosa,Martinez-Alcazar, M. Paz

, p. 859 - 868 (2007/10/03)

n-(N,N-Dimethylamino)phenylethynes were satisfactorily prepared by a Wittig reaction between chloromethylene(triphenyl)phosphine ylide and the appropriate n-(N,N-dimethylamino)benzaldehyde, followed by dehydrochlorination with a strong base. The conjugate

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