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Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1R,2R)(9CI) is a chiral chemical compound with the molecular formula C8H15NO2. It possesses two enantiomers that are non-superimposable mirror images of each other, making it a versatile building block in organic chemical synthesis and pharmaceutical research. The methyl ester form of Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1R,2R)- (9CI) facilitates its incorporation into various compounds and reactions, enhancing its utility in the development of new drugs and materials.

267230-45-5

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267230-45-5 Usage

Uses

Used in Organic Chemical Synthesis:
Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1R,2R)(9CI) is used as a key intermediate in the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable component in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1R,2R)(9CI) is utilized as a starting material for the development of new drugs. Its chiral nature allows for the exploration of the different biological activities of its enantiomers, potentially leading to the discovery of more effective and selective therapeutic agents.
Used in Chiral Chemistry:
The chiral properties of Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1R,2R)(9CI) make it an important compound in the field of chiral chemistry. It can be used to study the effects of stereochemistry on chemical reactions and to develop enantioselective synthetic methods, which are crucial for the production of enantiomerically pure compounds with specific biological activities.
Used in Drug Delivery Systems:
Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1R,2R)(9CI) can be incorporated into drug delivery systems to improve the bioavailability and targeting of therapeutic agents. Its ability to be easily modified and incorporated into various compounds makes it a promising candidate for the development of novel drug delivery platforms, such as nanoparticles, liposomes, and hydrogels, which can enhance the efficacy and safety of drug treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 267230-45-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,7,2,3 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 267230-45:
(8*2)+(7*6)+(6*7)+(5*2)+(4*3)+(3*0)+(2*4)+(1*5)=135
135 % 10 = 5
So 267230-45-5 is a valid CAS Registry Number.

267230-45-5SDS

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 methyl (1R,2R)-2-aminocyclohexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names (1R,2R)-Methyl 2-aminocyclohexanecarboxylate

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:267230-45-5 SDS

267230-45-5Relevant academic research and scientific papers

A New Ligand Scaffold for Catalytic Asymmetric Alkylzinc Additions to Aldehydes

Wipf, Peter,Wang, Xiaodong

, p. 1197 - 1199 (2007/10/03)

matrix presented 1,3-Azole derivatives of 2-aminocyclohexanecarboxylic acid represent a new class of bidentate ligands for metal-mediated catalytic asymmetric synthesis. N-[2-(4-Isopropyl-4,5-dihydrooxazol-2-yl)cyclohexyl]methanesulfonamide (6) is particu

Synthesis of substituted cyclohexenyl-based β-amino acids by ring-closing metathesis

Abell, Andrew D.,Gardiner, James

, p. 3663 - 3666 (2007/10/03)

(equation presented) A versatile ring-closing metathesis (RCM) approach has been developed for the preparation of cis and trans cyclohexenyl-based β-amino acids that are either unsubstituted (3) or substituted (10 and 12) at the α-position.

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