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17244-79-0

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17244-79-0 Usage

Chirality

Chiral molecule, exists in two mirror image forms

Physical state

White crystalline solid

Solubility

Sparingly soluble in water and organic solvents

Pharmaceutical applications

Commonly used as a precursor in the production of pharmaceuticals and other organic compounds

Drug synthesis

Used in the synthesis of analgesics, anticonvulsants, and antihistamines

Central nervous system activity

Ability to modify the activity of certain neurotransmitter systems in the central nervous system

Additional potential uses

Anti-inflammatory and anti-cancer agent (in some studies)

Enantiomers

Different biological activities may be present in the enantiomers, making stereochemistry important in pharmaceutical applications

Check Digit Verification of cas no

The CAS Registry Mumber 17244-79-0 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, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17244-79:
(7*1)+(6*7)+(5*2)+(4*4)+(3*4)+(2*7)+(1*9)=110
110 % 10 = 0
So 17244-79-0 is a valid CAS Registry Number.

17244-79-0SDS

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 1,2-diphenyl-2-pyrrolidin-1-ylethanol

1.2 Other means of identification

Product number -
Other names erythro-2-pyrrolidinyl-1,2-diphenylethanol

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:17244-79-0 SDS

17244-79-0Relevant 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

Towards phase-transfer catalysts with a chiral anion: Inducing asymmetry in the reactions of cations

Carter, Christabel,Fletcher, Sarah,Nelson, Adam

, p. 1995 - 2004 (2007/10/03)

The ability of chiral anions, for example bis[1,1′-bi-2-naphtholato]borate, to induce asymmetry in the reactions of prochiral cations was investigated. Ion-pairing of a borate anion with an aziridinium ion was demonstrated by NMR spectroscopy. The additio

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