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17244-82-5

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17244-82-5 Usage

General Description

2-(dimethylamino)-1,2-diphenylethanol is a chemical compound with a 3-carbon backbone, two phenyl groups, and a dimethylamino side chain. It is a tertiary amine that contains a hydroxyl group and is often used as a chiral auxiliary in organic synthesis. 2-(dimethylamino)-1,2-diphenylethanol has been studied for its potential as a chiral ligand in asymmetric catalysis and has shown promising results in promoting enantioselective transformations. Additionally, it has been used as a key intermediate in the production of pharmaceuticals and other fine chemicals. 2-(dimethylamino)-1,2-diphenylethanol is a versatile compound with a wide range of potential applications in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 17244-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,4 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17244-82:
(7*1)+(6*7)+(5*2)+(4*4)+(3*4)+(2*8)+(1*2)=105
105 % 10 = 5
So 17244-82-5 is a valid CAS Registry Number.

17244-82-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dimethylamino)-1,2-diphenylethanol

1.2 Other means of identification

Product number -
Other names (+-)-erythro-2-Dimethylamino-1,2-diphenyl-aethanol

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:17244-82-5 SDS

17244-82-5Relevant articles and documents

Hydrogen Bonding Phase-Transfer Catalysis with Potassium Fluoride: Enantioselective Synthesis of β-Fluoroamines

Pupo, Gabriele,Vicini, Anna Chiara,Ascough, David M. H.,Ibba, Francesco,Christensen, Kirsten E.,Thompson, Amber L.,Brown, John M.,Paton, Robert S.,Gouverneur, Véronique

supporting information, p. 2878 - 2883 (2019/02/14)

Potassium fluoride (KF) is an ideal reagent for fluorination because it is safe, easy to handle and low-cost. However, poor solubility in organic solvents coupled with limited strategies to control its reactivity has discouraged its use for asymmetric C-F

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