Carbamic acid, N-[2-(heptyloxy)phenyl]-, 2-(diethylamino)-1-methylethyl ester, hydrochloride (1:1)
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![Carbamic acid, N-[2-(heptyloxy)phenyl]-, 2-(diethylamino)-1-methylethyl ester, hydrochloride (1:1) structure](https://file.echemi.com/fileManage/upload/canonicalSmiles/20220812/f64f8d6edcb74fa6a921ef8368ff17d3.png "Carbamic acid, N-[2-(heptyloxy)phenyl]-, 2-(diethylamino)-1-methylethyl ester, hydrochloride (1:1)")
Carbamic acid, N-[2-(heptyloxy)phenyl]-, 2-(diethylamino)-1-methylethyl ester, hydrochloride (1:1)
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CAS No:
68931-03-3
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Formula:
C21H36N2O3.ClH
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Chemical Name:
Carbamic acid, N-[2-(heptyloxy)phenyl]-, 2-(diethylamino)-1-methylethyl ester, hydrochloride (1:1)
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Synonyms:
Carbamic acid,N-[2-(heptyloxy)phenyl]-,2-(diethylamino)-1-methylethyl ester,hydrochloride (1:1);Carbamic acid,[2-(heptyloxy)phenyl]-,2-(diethylamino)-1-methylethyl ester,monohydrochloride;BK 95;Carbisocaine
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CAS No:
Carbamic acid, N-[2-(heptyloxy)phenyl]-, 2-(diethylamino)-1-methylethyl ester, hydrochloride (1:1) Basic Attributes
401.0 g/mol
400.2492707 g/mol
Drug Information
Drugs that block nerve conduction when applied locally to nerve tissue in appropriate concentrations. They act on any part of the nervous system and on every type of nerve fiber. In contact with a nerve trunk, these anesthetics can cause both sensory and motor paralysis in the innervated area. Their action is completely reversible. (From Gilman AG, et. al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed) Nearly all local anesthetics act by reducing the tendency of voltage-dependent sodium channels to activate. (See all compounds classified as Anesthetics, Local.)
carbisocaine
Computed Properties
Molecular Weight:401.0
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:14
Exact Mass:400.2492707
Monoisotopic Mass:400.2492707
Topological Polar Surface Area:52
Heavy Atom Count:27
Complexity:361
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes
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