1.0 2016-09-30 22:53:36 UTC 2020-04-22 15:10:30 UTC BMDB0002284 BMDB02284 N-Acetylcadaverine Monoacetyl cadaverine Monoacetylcadaverine Acetylcadaverine N-(5-Aminopentyl)acetamide C7H16N2O 144.2147 144.126263144 N-(5-aminopentyl)acetamide N-acetylcadaverine 32343-73-0 CC(=O)NCCCCCN InChI=1S/C7H16N2O/c1-7(10)9-6-4-2-3-5-8/h2-6,8H2,1H3,(H,9,10) RMOIHHAKNOFHOE-UHFFFAOYSA-N belongs to the class of organic compounds known as acetamides. These are organic compounds with the general formula RNHC(=O)CH3, where R= organyl group. Organic compounds Organic acids and derivatives Carboxylic acids and derivatives Carboxylic acid derivatives Acetamides Amino acids and derivatives Carbonyl compounds Hydrocarbon derivatives Monoalkylamines Organic oxides Organopnictogen compounds Secondary carboxylic acid amides Acetamide Aliphatic acyclic compound Amine Amino acid or derivatives Carbonyl group Hydrocarbon derivative Organic nitrogen compound Organic oxide Organic oxygen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Primary aliphatic amine Primary amine Secondary carboxylic acid amide Aliphatic acyclic compounds Solid logp -0.40 ALOGPS logs -0.78 ALOGPS logp -0.58 ChemAxon pka_strongest_acidic 16.53 ChemAxon pka_strongest_basic 10.21 ChemAxon iupac N-(5-aminopentyl)acetamide ChemAxon average_mass 144.2147 ChemAxon mono_mass 144.126263144 ChemAxon smiles CC(=O)NCCCCCN ChemAxon formula C7H16N2O ChemAxon inchi InChI=1S/C7H16N2O/c1-7(10)9-6-4-2-3-5-8/h2-6,8H2,1H3,(H,9,10) ChemAxon inchikey RMOIHHAKNOFHOE-UHFFFAOYSA-N ChemAxon polar_surface_area 55.12 ChemAxon refractivity 41.42 ChemAxon polarizability 17.36 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 2 ChemAxon donor_count 2 ChemAxon physiological_charge 1 ChemAxon formal_charge 0 ChemAxon number_of_rings 0 ChemAxon bioavailability 1 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Specdb::MsMs 100776 Specdb::MsMs 100777 Specdb::MsMs 100778 Specdb::MsMs 166218 Specdb::MsMs 166219 Specdb::MsMs 166220 Specdb::MsMs 2840703 Specdb::MsMs 2840704 Specdb::MsMs 2840705 Specdb::MsMs 2865081 Specdb::MsMs 2865082 Specdb::MsMs 2865083 Specdb::MsIr 1719 Specdb::MsIr 1720 Specdb::MsIr 1721 Specdb::CMs 11182 Specdb::CMs 148905 Specdb::NmrOneD 115978 Specdb::NmrOneD 115979 Specdb::NmrOneD 115980 Specdb::NmrOneD 115981 Specdb::NmrOneD 115982 Specdb::NmrOneD 115983 Specdb::NmrOneD 115984 Specdb::NmrOneD 115985 Specdb::NmrOneD 115986 Specdb::NmrOneD 115987 Specdb::NmrOneD 115988 Specdb::NmrOneD 115989 Specdb::NmrOneD 115990 Specdb::NmrOneD 115991 Specdb::NmrOneD 115992 Specdb::NmrOneD 115993 Specdb::NmrOneD 115994 Specdb::NmrOneD 115995 Specdb::NmrOneD 115996 Specdb::NmrOneD 115997 FDB022947 164295 189087 88824 Sugita, Yuzo; Yoshimura, Yoshinori; Okada, Masato. Manufacture of monoacetylpolyamines with diacetylpolyamine amidohydrolase or microorganisms. Jpn. Kokai Tokkyo Koho (1992), 11 pp. CODEN: JKXXAF JP 04234992 A 19920824 Heisei. CAN 118:21079 AN 1993:21079