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2-Pyrrolidineethanol, R, 1-dimethyl-, (RS,2R)- is a complex organic compound with the chemical formula C7H15NO. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it exists in two enantiomeric forms: (RS,2R)- and (RS,2S)-. 2-Pyrrolidineethanol,R,1-dimethyl-,(RS,2R)- is a derivative of pyrrolidine, a heterocyclic amine, with an ethanol group attached to the 2-position and two methyl groups at the 1-position. It is used in various chemical and pharmaceutical applications, such as a building block for the synthesis of more complex molecules and as an intermediate in the production of certain drugs. Due to its chiral nature, the specific enantiomer used in these applications can significantly impact the effectiveness and safety of the final product.

496-48-0

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496-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 496-48-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 496-48:
(5*4)+(4*9)+(3*6)+(2*4)+(1*8)=90
90 % 10 = 0
So 496-48-0 is a valid CAS Registry Number.

496-48-0SDS

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 (+)-pseudohygroline

1.2 Other means of identification

Product number -
Other names (S)-1-((R)-1-Methyl-pyrrolidin-2-yl)-propan-2-ol

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:496-48-0 SDS

496-48-0Downstream Products

496-48-0Relevant academic research and scientific papers

Electroorganic Chemistry. 46. A New Carbon-Carbon Bond Forming Reaction at the α-Position of Amines Utilizing Anodic Oxidation as a Key Step

Shono, Tatsuya,Matsumura, Yoshihiro,Tsubata, Kenji

, p. 1172 - 1176 (2007/10/02)

A new carbon-carbon bond forming reaction at the α-position of primary and secondary amines has been exploited.The method involves anodic oxidation of urethanes derived from the primary and secondary amines and subsequent acid-catalyzed reaction of the re

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