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Home > Encyclopedia > 4-(1-aminoethyl)-N-pyridin-4-ylcyclohexane-1-carboxamide;dihydrochloride

4-(1-aminoethyl)-N-pyridin-4-ylcyclohexane-1-carboxamide;dihydrochloride

4-(1-aminoethyl)-N-pyridin-4-ylcyclohexane-1-carboxamide;dihydrochloride structure

4-(1-aminoethyl)-N-pyridin-4-ylcyclohexane-1-carboxamide;dihydrochloride 

structure
  • CAS No:

    138381-45-0

  • Formula:

    C14H23Cl2N3O

  • Chemical Name:

    4-(1-aminoethyl)-N-pyridin-4-ylcyclohexane-1-carboxamide;dihydrochloride

  • Synonyms:

    N-(4-pyridyl)-4-(1-aminoethyl)cyclohexanecarboxamide;Y 27632;Y 27632, (4(R)-trans)-isomer;Y 27632, (4(S)-trans)-isomer;Y 27632, (trans)-isomer;Y 27632, dihydrochloride, (4(R)-trans)-isomer;Y-27632;Y27632;138381-45-0;Cyclohexanecarboxamide, 4-(1-aminoethyl)-N-4-pyridinyl-, dihydrochloride;N-(4-Pyridyl)-4-(1-aminoethyl)cyclohexanecarboxamide dihydrochloride;Y27632 (hydrochloride);SCHEMBL1165652;SCHEMBL1554110;DTXSID20930097;BCP06536;AKOS026750185;CCG-221637;LP00333;AK198669;EU-0100333;FT-0771389;Y 0503;SR-01000075205;SR-01000075205-1;4-(1-aminoethyl)-N-(4-pyridyl)cyclohexanecarboxamide di-hydrochloride;4-(1-AMINOETHYL)-N-(PYRIDIN-4-YL)CYCLOHEXANE-1-CARBOXAMIDE DIHYDROCHLORIDE;4-[(1R)-1-aminoethyl]-N-pyridin-4-ylcyclohexane-1-carboxamide;dihydrochloride;trans-4-(1-aminoethyl)-N-(4-pyridyl) cyclohexane carboxamide dihydrochloride;4-(1-Aminoethyl)-N-(pyridin-4(1H)-ylidene)cyclohexane-1-carboxamide--hydrogen chloride (1/2)

4-(1-aminoethyl)-N-pyridin-4-ylcyclohexane-1-carboxamide;dihydrochloride Basic Attributes

320.3 g/mol

319.1218178 g/mol

Characteristics

68 Ų

Safety Information

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction. (See all compounds classified as Enzyme Inhibitors.)|Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS. (See all compounds classified as Antihypertensive Agents.)|A heterogeneous group of drugs used to produce muscle relaxation, excepting the neuromuscular blocking agents. They have their primary clinical and therapeutic uses in the treatment of muscle spasm and immobility associated with strains, sprains, and injuries of the back and, to a lesser degree, injuries to the neck. They have been used also for the treatment of a variety of clinical conditions that have in common only the presence of skeletal muscle hyperactivity, for example, the muscle spasms that can occur in MULTIPLE SCLEROSIS. (From Smith and Reynard, Textbook of Pharmacology, 1991, p358) (See all compounds classified as Muscle Relaxants, Central.)

N-(4-pyridyl)-4-(1-aminoethyl)cyclohexanecarboxamide

Computed Properties

Molecular Weight:320.3
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:319.1218178
Monoisotopic Mass:319.1218178
Topological Polar Surface Area:68
Heavy Atom Count:20
Complexity:268
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:3
Compound Is Canonicalized:Yes

Guide of 4-(1-aminoethyl)-N-pyridin-4-ylcyclohexane-1-carboxamide;dihydrochloride

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