1.0 2016-09-30 23:22:06 UTC 2020-04-22 15:17:28 UTC BMDB0006458 BMDB06458 D-Lactaldehyde D-2-Hydroxypropionaldehyde (2R)-2-Hydroxypropanal (R)-Lactaldehyde C3H6O2 74.0785 74.036779436 (2R)-2-hydroxypropanal D-lactaldehyde 3946-09-6 C[C@@H](O)C=O InChI=1S/C3H6O2/c1-3(5)2-4/h2-3,5H,1H3/t3-/m1/s1 BSABBBMNWQWLLU-GSVOUGTGSA-N belongs to the class of organic compounds known as alpha-hydroxyaldehydes. These are organic compounds containing an aldehyde substituted with a hydroxyl group on the adjacent carbon. Organic compounds Organic oxygen compounds Organooxygen compounds Carbonyl compounds Alpha-hydroxyaldehydes Hydrocarbon derivatives Organic oxides Secondary alcohols Short-chain aldehydes Alcohol Aliphatic acyclic compound Alpha-hydroxyaldehyde Hydrocarbon derivative Organic oxide Secondary alcohol Short-chain aldehyde Aliphatic acyclic compounds lactaldehyde Solid logp -1.04 ALOGPS logs 0.95 ALOGPS logp -0.63 ChemAxon pka_strongest_acidic 14 ChemAxon pka_strongest_basic -3.2 ChemAxon iupac (2R)-2-hydroxypropanal ChemAxon average_mass 74.0785 ChemAxon mono_mass 74.036779436 ChemAxon smiles C[C@@H](O)C=O ChemAxon formula C3H6O2 ChemAxon inchi InChI=1S/C3H6O2/c1-3(5)2-4/h2-3,5H,1H3/t3-/m1/s1 ChemAxon inchikey BSABBBMNWQWLLU-GSVOUGTGSA-N ChemAxon polar_surface_area 37.3 ChemAxon refractivity 17.91 ChemAxon polarizability 7.19 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 2 ChemAxon donor_count 1 ChemAxon physiological_charge 0 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 Pyruvate Metabolism SMP0087231 Specdb::MsMs 25751 Specdb::MsMs 25752 Specdb::MsMs 25753 Specdb::MsMs 32309 Specdb::MsMs 32310 Specdb::MsMs 32311 Specdb::MsMs 2798753 Specdb::MsMs 2798754 Specdb::MsMs 2798755 Specdb::MsMs 2883299 Specdb::MsMs 2883300 Specdb::MsMs 2883301 Specdb::CMs 3115 Specdb::CMs 39017 Specdb::CMs 174947 Specdb::NmrOneD 150200 Specdb::NmrOneD 150201 Specdb::NmrOneD 150202 Specdb::NmrOneD 150203 Specdb::NmrOneD 150204 Specdb::NmrOneD 150205 Specdb::NmrOneD 150206 Specdb::NmrOneD 150207 Specdb::NmrOneD 150208 Specdb::NmrOneD 150209 Specdb::NmrOneD 150210 Specdb::NmrOneD 150211 Specdb::NmrOneD 150212 Specdb::NmrOneD 150213 Specdb::NmrOneD 150214 Specdb::NmrOneD 150215 Specdb::NmrOneD 150216 Specdb::NmrOneD 150217 Specdb::NmrOneD 150218 Specdb::NmrOneD 150219 FDB023918 388473 439350 17167 C00937 CPD-358 36414 Lactaldehyde Lobell, Mario, Grout, David H. G. New insight into the pyruvate decarboxylase-catalyzed formation of lactaldehyde from H-D exchange experiments: a 'water proof' active site. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1996), (13), 1577-1581; Kranz, Cyrill. Synthesis of Lactic Aldehyde. Chemicke Listy pro Vedu a Prumysl (1912), 5 323-7.