1.0 2016-09-30 22:31:13 UTC 2020-04-22 15:03:45 UTC BMDB0000473 BMDB00473 6-Dimethylaminopurine 6-(Dimethylamino)purine 6-Dimethyladenine N,N-Dimethyl-1H-purin-6-amine N,N-Dimethyl-6-aminopurine N,N-Dimethyladenine N(6)-Dimethyladenine 6,6-Dimethyladenine 6-(Dimethylamino)-purine 6-Dimethylamine purine Dimethyladenine DMAP N,N-Dimethyl-adenine N6,N6-Dimethyl-adenine N6,N6-Dimethyladenine 6-DMAP Dimethylaminopurine N(6),N(6)-Dimethyladenine 6-Dimethylaminopurine C7H9N5 163.1799 163.085795313 N,N-dimethyl-7H-purin-6-amine 6-(dimethylamino)-purine 938-55-6 CN(C)C1=NC=NC2=C1NC=N2 InChI=1S/C7H9N5/c1-12(2)7-5-6(9-3-8-5)10-4-11-7/h3-4H,1-2H3,(H,8,9,10,11) BVIAOQMSVZHOJM-UHFFFAOYSA-N belongs to the class of organic compounds known as 6-alkylaminopurines. 6-alkylaminopurines are compounds that contain an alkylamine group attached at the 6-position of a purine. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring. Organic compounds Organoheterocyclic compounds Imidazopyrimidines Purines and purine derivatives 6-alkylaminopurines Aminopyrimidines and derivatives Azacyclic compounds Dialkylarylamines Heteroaromatic compounds Hydrocarbon derivatives Imidazoles Imidolactams Organopnictogen compounds 6-alkylaminopurine Aminopyrimidine Aromatic heteropolycyclic compound Azacycle Azole Dialkylarylamine Heteroaromatic compound Hydrocarbon derivative Imidazole Imidolactam Organic nitrogen compound Organonitrogen compound Organopnictogen compound Pyrimidine Aromatic heteropolycyclic compounds tertiary amine Solid logp 0.53 ALOGPS logs -1.73 ALOGPS logp 0.36 ChemAxon pka_strongest_acidic 10.19 ChemAxon pka_strongest_basic 3.35 ChemAxon iupac N,N-dimethyl-7H-purin-6-amine ChemAxon average_mass 163.1799 ChemAxon mono_mass 163.085795313 ChemAxon smiles CN(C)C1=NC=NC2=C1NC=N2 ChemAxon formula C7H9N5 ChemAxon inchi InChI=1S/C7H9N5/c1-12(2)7-5-6(9-3-8-5)10-4-11-7/h3-4H,1-2H3,(H,8,9,10,11) ChemAxon inchikey BVIAOQMSVZHOJM-UHFFFAOYSA-N ChemAxon polar_surface_area 57.7 ChemAxon refractivity 47.95 ChemAxon polarizability 16.32 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 4 ChemAxon donor_count 1 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon number_of_rings 2 ChemAxon bioavailability 1 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Specdb::CMs 13979 Specdb::CMs 136020 Specdb::CMs 143754 Specdb::MsIr 549 Specdb::MsIr 550 Specdb::MsIr 551 Specdb::NmrTwoD 1330 Specdb::MsMs 689 Specdb::MsMs 690 Specdb::MsMs 691 Specdb::MsMs 7859 Specdb::MsMs 7860 Specdb::MsMs 7861 Specdb::MsMs 14531 Specdb::MsMs 14532 Specdb::MsMs 14533 Specdb::MsMs 2331207 Specdb::MsMs 2331208 Specdb::MsMs 2331209 Specdb::MsMs 2631341 Specdb::MsMs 2631342 Specdb::MsMs 2631343 Specdb::NmrOneD 1386 Specdb::NmrOneD 144130 Specdb::NmrOneD 144131 Specdb::NmrOneD 144132 Specdb::NmrOneD 144133 Specdb::NmrOneD 144134 Specdb::NmrOneD 144135 Specdb::NmrOneD 144136 Specdb::NmrOneD 144137 Specdb::NmrOneD 144138 Specdb::NmrOneD 144139 Specdb::NmrOneD 144140 Specdb::NmrOneD 144141 Specdb::NmrOneD 144142 Specdb::NmrOneD 144143 Specdb::NmrOneD 144144 Specdb::NmrOneD 144145 Specdb::NmrOneD 144146 Specdb::NmrOneD 144147 Specdb::NmrOneD 144148 Specdb::NmrOneD 144149 3022 FDB022062 3134 C00032053 60281 5460 Baker, B. R.; Joseph, Joseph P.; Schaub, Robert E. Puromycin. Synthetic studies. I. Synthesis of 6-dimethylaminopurine, a hydrolytic fragment. Journal of Organic Chemistry (1954), 19 631-7.