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63246-63-9

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63246-63-9 Usage

General Description

2-(dimethylamino)-2-methylpropane-1,3-diol is a chemical compound with the molecular formula C7H17NO2. It is a tertiary amine with a hydroxyl group, making it an amino alcohol. 2-(dimethylamino)-2-methylpropane-1,3-diol is commonly used as a chiral auxiliary in organic synthesis, particularly in the preparation of chiral aldehydes and ketones. It is also utilized as a reagent for the synthesis of various pharmaceutical compounds and agrochemicals. Additionally, 2-(dimethylamino)-2-methylpropane-1,3-diol has been studied for its potential applications in the field of asymmetric synthesis and catalysis.

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 articles and documents

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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