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2-(dimethylamino)-2-methylpropane-1,3-diol is a chemical compound characterized by the molecular formula C7H17NO2. It is a tertiary amine with a hydroxyl group, classifying it as an amino alcohol. 2-(dimethylamino)-2-methylpropane-1,3-diol is known for its role in various chemical processes and applications, particularly in the synthesis of chiral molecules and the development of pharmaceutical and agrochemical products.

63246-63-9

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63246-63-9 Usage

Uses

Used in Organic Synthesis:
2-(dimethylamino)-2-methylpropane-1,3-diol is utilized as a chiral auxiliary in organic synthesis, specifically for the preparation of chiral aldehydes and ketones. Its unique structure allows for the creation of enantioselective reactions, which is crucial for producing compounds with specific stereochemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-(dimethylamino)-2-methylpropane-1,3-diol serves as a reagent for the synthesis of various pharmaceutical compounds. Its ability to influence the stereochemistry of synthesized products makes it a valuable tool in the development of drugs with desired biological activities and reduced side effects.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 2-(dimethylamino)-2-methylpropane-1,3-diol is employed for the synthesis of agrochemicals with specific chiral properties. This ensures the effectiveness of these compounds in agricultural applications while minimizing potential environmental impacts.
Used in Asymmetric Synthesis:
2-(dimethylamino)-2-methylpropane-1,3-diol has been studied for its potential applications in asymmetric synthesis, a field that focuses on the production of enantiomerically pure compounds. Its use in this area can lead to the development of more efficient and selective synthetic routes.
Used in Catalysis:
Furthermore, research into the applications of 2-(dimethylamino)-2-methylpropane-1,3-diol in catalysis is ongoing. Its potential as a catalyst or catalyst precursor could enhance the efficiency of various chemical reactions, particularly those involving the formation of chiral centers.

Check Digit Verification of cas no

The CAS Registry Mumber 63246-63-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,4 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 63246-63:
(7*6)+(6*3)+(5*2)+(4*4)+(3*6)+(2*6)+(1*3)=119
119 % 10 = 9
So 63246-63-9 is a valid CAS Registry Number.

63246-63-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dimethylamino)-2-methylpropane-1,3-diol

1.2 Other means of identification

Product number -
Other names 2-dimethylamino-2-methyl-1,3-propandiol

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:63246-63-9 SDS

63246-63-9Downstream Products

63246-63-9Relevant academic research and scientific papers

PROCESS FOR MAKING TERTIARY AMINOALCOHOL COMPOUNDS

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Page/Page column 15, (2012/04/17)

Provided is a process for making a tertiary aminoalcohol compound. The process comprises using an excess amount of a carbonyl compound in a condensation step between the carbonyl compound and a nitroalkane, and conducting a hydrogenation/alkylation step to produce the tertiary aminoalcohol. The process uses fewer steps than conventional processes.

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