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3-(Cyclohexyloxy)propan-1-amine, also known as CHOPA, is an organic compound with the chemical formula C9H19NO. It is a primary aliphatic amine, with a cyclohexyl group attached to the nitrogen atom. CHOPA is commonly used as a building block in organic synthesis and can be utilized in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. It has also been studied as a potential ligand in the synthesis of metal-organic frameworks and coordination compounds due to its unique structural and chemical properties. Additionally, CHOPA may have potential applications in the field of material science and as a reagent in organic chemistry reactions.

16728-63-5

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16728-63-5 Usage

Uses

Used in Pharmaceutical Industry:
3-(Cyclohexyloxy)propan-1-amine is used as a building block for the synthesis of various pharmaceuticals, due to its unique structural and chemical properties.
Used in Agrochemical Industry:
3-(Cyclohexyloxy)propan-1-amine is used as a building block for the synthesis of agrochemicals, contributing to the development of new and effective products.
Used in Specialty Chemicals Industry:
3-(Cyclohexyloxy)propan-1-amine is used as a building block for the production of specialty chemicals, enhancing the properties and performance of these chemicals.
Used in Metal-Organic Frameworks and Coordination Compounds:
3-(Cyclohexyloxy)propan-1-amine is used as a potential ligand in the synthesis of metal-organic frameworks and coordination compounds, due to its unique structural and chemical properties.
Used in Material Science:
3-(Cyclohexyloxy)propan-1-amine may have potential applications in the field of material science, contributing to the development of new materials with improved properties.
Used as a Reagent in Organic Chemistry Reactions:
3-(Cyclohexyloxy)propan-1-amine is used as a reagent in various organic chemistry reactions, facilitating the synthesis of complex organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 16728-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,2 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16728-63:
(7*1)+(6*6)+(5*7)+(4*2)+(3*8)+(2*6)+(1*3)=125
125 % 10 = 5
So 16728-63-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H19NO/c10-7-4-8-11-9-5-2-1-3-6-9/h9H,1-8,10H2

16728-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-cyclohexyloxypropan-1-amine

1.2 Other means of identification

Product number -
Other names 3-Cyclohexyloxypropylamin

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:16728-63-5 SDS

16728-63-5Relevant academic research and scientific papers

Development of dual-acting agents for thromboxane receptor antagonism and thromboxane synthase inhibition. 3. Synthesis and biological activities of oxazolecarboxamide-substituted ω-phenyl-ω-(3-pyridyl)alkenoic acid derivatives and related compounds

Takeuchi, Kumiko,Kohn, Todd J.,True, Timothy A.,Mais, Dale E.,Wikel, James H.,Utterback, Barbara G.,Wyss, Virginia L.,Jakubowski, Joseph A.

, p. 5362 - 5374 (2007/10/03)

A novel series of oxazolecarboxamide-substituted ω-phenyl-ω-(3- pyridyl)alkenoic acid derivatives was discovered as potent dual-acting agents to block the TXA2 receptor and to inhibit the thromboxane synthase (TRA/TSI). Synthesis, structure-activity relationship (SAR), and in vitro and in vivo pharmacology of this series of compounds are described. Modification of the series revolved around the oxazole moiety to increase the hydrophilicity of the compounds and to correlate the biological activity with lipophilicity of the compounds. The most potent in the series was (E)-7-[4- [4-[[(4-cyclohexylbutyl)amino]carbonyl]-2-oxazolyl]phenyl]-7-(3-pyridyl)hept- 6-enoic acid (14) with K(d) = 9.9 ± 0.4 nM for the thromboxane receptor antagonism and IC50 = 55.0 ± 17.9 nM for thromboxane synthase inhibition. The compound 14 was a selective TRA/TSI which exhibited desirable characteristics for oral activity, 'shunt' effect to elevate PGI2 level, and absence of agonist activity.

Carbamoyl substituted heterocycles

-

, (2008/06/13)

This invention relates to carbamoyl substituted heterocycles which are ω-phenyl-ω-(3-pyridyl)-ω-alkenoic acid derivatives bearing a carbamoyl substituted oxazolyl or oxazolinyl group on the phenyl ring and which demonstrate utility for thromboxane receptor antagonism and/or thromboxane synthase inhibition, as well as pharmaceutical formulations containing them, methods for their use, and processes and intermediates for their preparation.

PREPARATION OF SUBSTITUTED ALKENOIC ACIDS

-

, (2008/06/13)

This invention relates to a highly selective process for preparation of E-ω-phenyl-ω-(3-pyridyl)-ω-alkenoic acid derivatives bearing a carbamoyl substituted oxazolyl or oxazolinyl group on the phenyl ring which demonstrate utility for thromboxane receptor antagonism and/or thromboxane synthase inhibition, as well as to intermediates therefor.

Carbamoyl substituted oxazoles as thromboxane receptor antagonists

-

, (2008/06/13)

This invention relates to carbamoyl substituted heterocycles which are ω-phenyl-ω-(3-pyridyl)-ω-alkenoic acid derivatives bearing a carbamoyl substituted oxazolyl or oxazolinyl group on the phenyl ring and which demonstrate utility for thromboxane receptor antagonism and/or thromboxane synthase inhibition, as well as pharmaceutical formulations containing them, methods for their use, and processes and intermediates for their preparation.

Polycyclic amines and intermediates therefor

-

, (2008/06/13)

This invention relates to a new method for the preparation of amines containing alkylene groups by using cyclic alkylene sulphuric esters, and novel intermediates for use in the method. The new method is useful for preparation of i.a. pharmaceuticals. The novel intermediates are useful i.a. as surfactants.

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