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(R)-Methyl nipecotate, also known as Methyl (2R)-2-pyridinecarboxylate, is a chiral chemical compound belonging to the class of pyridines or heterocyclic compounds. It features a pyridine ring, which is a six-membered aromatic compound composed of five carbon atoms and one nitrogen atom. The presence of a chiral center in the molecule results in two enantiomers, which can be significant in asymmetric reactions. Highly soluble, (R)-Methyl nipecotate should be stored in a cool, dry place under an inert atmosphere to prevent degradation. It is important to handle (R)-Methyl nipecotate with care, as it can be harmful if swallowed or if it comes into contact with skin or eyes. (R)-Methyl nipecotate's precise effects and uses are still under investigation in various research activities, particularly in the fields of chemical and pharmaceutical research.

164323-85-7

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164323-85-7 Usage

Uses

Used in Chemical Research:
(R)-Methyl nipecotate is used as a chiral building block for the synthesis of various organic compounds. Its unique structure and the presence of a chiral center make it a valuable component in the development of enantioselective reactions and the creation of new chiral molecules.
Used in Pharmaceutical Research:
(R)-Methyl nipecotate is employed as an intermediate in the synthesis of pharmaceutical compounds. Its chiral nature allows for the development of enantiomerically pure drugs, which can exhibit different biological activities and reduce potential side effects associated with racemic mixtures.
Used in Asymmetric Catalysis:
(R)-Methyl nipecotate is utilized as a ligand or catalyst in asymmetric catalysis, a technique that enables the selective formation of one enantiomer over the other. This is crucial in the production of enantiomerically pure compounds, which are often required for pharmaceutical applications.
Used in Analytical Chemistry:
(R)-Methyl nipecotate can be used as a chiral reference standard in analytical chemistry. Its distinct enantiomers can be used to calibrate instruments and develop methods for the separation and identification of chiral compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 164323-85-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,3,2 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 164323-85:
(8*1)+(7*6)+(6*4)+(5*3)+(4*2)+(3*3)+(2*8)+(1*5)=127
127 % 10 = 7
So 164323-85-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO2/c1-10-7(9)6-3-2-4-8-5-6/h6,8H,2-5H2,1H3/t6-/m1/s1

164323-85-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-Methyl piperidine-3-carboxylate

1.2 Other means of identification

Product number -
Other names methyl (3R)-piperidine-3-carboxylate

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:164323-85-7 SDS

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