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90704-69-1

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90704-69-1 Usage

Description

1-(2,3-dimethoxyphenyl)-N,N-dimethylmethanamine is a chemical compound characterized by the molecular formula C11H17NO2. It is a tertiary amine with two methyl groups and a 2,3-dimethoxyphenyl group attached to the nitrogen atom. 1-(2,3-dimethoxyphenyl)-N,N-dimethylmethanamine is known for its applications in organic synthesis and pharmaceutical research, where it serves as a versatile reagent. Due to its potential therapeutic applications, it has been the subject of various studies aimed at understanding its efficacy in treating different medical conditions. However, it is crucial to handle this chemical with care, as it may present health risks and environmental hazards if not managed properly.

Uses

Used in Organic Synthesis:
1-(2,3-dimethoxyphenyl)-N,N-dimethylmethanamine is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions. Its unique structure allows it to participate in a range of reactions, making it a valuable tool in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(2,3-dimethoxyphenyl)-N,N-dimethylmethanamine is used as a reagent for the development of new drugs. Its potential therapeutic applications are being explored in the treatment of various medical conditions, making it an important compound in the search for novel pharmaceutical agents.
Used in the Treatment of Medical Conditions:
1-(2,3-dimethoxyphenyl)-N,N-dimethylmethanamine has been studied for its potential use as a therapeutic agent in the treatment of various medical conditions. Its specific applications are still under investigation, but the compound's unique properties make it a promising candidate for further research and development in the medical field.

Check Digit Verification of cas no

The CAS Registry Mumber 90704-69-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,0 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90704-69:
(7*9)+(6*0)+(5*7)+(4*0)+(3*4)+(2*6)+(1*9)=131
131 % 10 = 1
So 90704-69-1 is a valid CAS Registry Number.

90704-69-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethoxy-N,N-dimethyl-Benzenemethanamine

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:90704-69-1 SDS

90704-69-1Relevant articles and documents

Synthesis and oxidation-induced DNA cross-linking capabilities of bis(catechol) quaternary ammonium derivatives

Song, Zhibin,Weng, Xiaocheng,Weng, Liwei,Huang, Jing,Wang, Xiaolin,Bai, Minghui,Zhou, Yangyang,Yang, Guangfu,Zhou, Xiang

supporting information; experimental part, p. 5751 - 5754 (2009/05/31)

A study was conducted to demonstrate the synthesis of a number of DNA crosslinking agents, such as bis(catechol) quaternary ammonium derives. It was found that these agents can crosslink DNA through an o-quinone intermediate, induced by oxidation. It was also found that these compounds are composed of two catechol monomers, acting as DNA cross-linking units and are joined by different linkers that act as DNA binding units. Positive charged linkers and quaternary ammonium derivatives were used in the study, to achieve high affinity to DNA. Aliphatic and aromatic chains were investigated, to determine their ability in performing favorable cross-linking reactions and to determine the relationship between agent flexibility and DNA cross-linking abilities.

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