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53663-37-9

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53663-37-9 Usage

General Description

3-(dimethoxymethyl)aniline is a chemical compound with the molecular formula C9H13NO2. It is a derivative of aniline, with two methoxy groups and a methyl group attached to the carbon atoms. 3-(dimethoxymethyl)aniline is commonly used as an intermediate or building block in the synthesis of various organic compounds, including pharmaceuticals, dyes, and polymers. It is typically a pale yellow to brown liquid with a strong odor, and it is considered to be moderately toxic and a skin and eye irritant. 3-(dimethoxymethyl)aniline should be handled with care and stored in a cool, dry place away from direct sunlight and heat sources. Overall, this compound plays a significant role in organic synthesis and has various industrial applications.

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

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