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N-(2-hydroxyethyl)dodecanamide

PubChem CID: 8899

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Compound Synonyms N-(2-HYDROXYETHYL)DODECANAMIDE, 142-78-9, Lauric acid monoethanolamide, Lauramide MEA, N-Lauroylethanolamine, Laurylethanolamide, Lauric monoethanolamide, Amisol LDE, Copramyl, Dodecanamide, N-(2-hydroxyethyl)-, Vistalan, N-(2-Hydroxyethyl)lauramide, Ultrapole H, Comperlan LM, Cyclomide LM, Lauridit LM, Lauroyl-EA, Rolamid CM, Stabilor CMH, Crillon LME, Lauric ethylolamide, Lauroyl monoethanolamide, Steinamid L 203, 2-Dodecanamidoethanol, Rewomid L 203, Laurylamidoethanol, Amisol LME, Lauric acid ethanolamide, Lauryl ethanolamide, Lauric acid monoethanolamine, Lauric N-(2-hydroxyethyl)amide, Lauroyl-ethanolamine, Monoethanolamine lauric acid amide, CCRIS 4834, HSDB 5644, EINECS 205-560-1, N-(Dodecanoyl)-ethanolamine, Lauryl monoethanolamide, 098P2IGT76, MFCD00020561, N-(dodecanoyl)ethanolamine, DTXSID5025493, LAURAMIDE MONOETHANOLAMIDE, N-(2-Hydroxyethyl)dodecaneamide, CHEBI:85263, NAE 12:0, N-(2-HYDROXYETHYL)DODECANAMIDE [HSDB], Dodecylethanol amide, Coconut monoethanolamide, UNII-098P2IGT76, Incromide LCL, Mackamide LMM, Ablumide LME, Hartamide LMEA, Lauroylethanolamide, 2Dodecanamidoethanol, NAE, Stabilor C.M.H., Crillon L.M.E., Alkamide L-203, dodecanoyl ethanolamide, 1:1 Cocamide MEA, 1:1 Lauramide MEA, N-dodecanoylethanolamine, N-LEA, N(2Hydroxyethyl)lauramide, Empilan LME (Salt/Mix), Lauramide-MEA (1:1), ALKAMIDE L 203, N(2Hydroxyethyl)dodecanamide, Lauric N(2hydroxyethyl)amide, LAURAMIDE MEA [INCI], SCHEMBL679082, TOHOL N 120, CHEMBL246914, Dodecanamide, N(2hydroxyethyl), DTXCID205493, Cocomonoethanolamide (Salt/Mix), Dodecanamide, N-2-hydroxyethyl-, LMFA08040041, XH0834, AKOS010638882, CS-W022897, DS-2807, lauric acid monoethanolamide, AldrichCPR, N-(BETA-HYDROXYETHYL)DODECANAMIDE, SY110473, NS00005328, EN300-7367571, Q27158443, Z808715244, 205-560-1
Ghose Rule True
Classyfire Kingdom Organic compounds
Topological Polar Surface Area 49.3
Hydrogen Bond Donor Count 2.0
Pfizer 3 75 Rule False
Np Classifier Class N-acyl ethanolamines (endocannabinoids)
Deep Smiles CCCCCCCCCCCC=O)NCCO
Heavy Atom Count 17.0
Classyfire Class Carboximidic acids and derivatives
Classyfire Subclass Carboximidic acids
Isotope Atom Count 0.0
Molecular Complexity 172.0
Database Name imppat_phytochem;pubchem
Defined Atom Stereocenter Count 0.0
Iupac Name N-(2-hydroxyethyl)dodecanamide
Veber Rule False
Classyfire Superclass Organic acids and derivatives
Xlogp 4.0
Gsk 4 400 Rule True
Molecular Formula C14H29NO2
Inchi Key QZXSMBBFBXPQHI-UHFFFAOYSA-N
Silicos It Class Moderately soluble
Rotatable Bond Count 12.0
Synonyms amisol lde
Esol Class Soluble
Functional Groups CNC(C)=O, CO
Compound Name N-(2-hydroxyethyl)dodecanamide
Exact Mass 243.22
Formal Charge 0.0
Monoisotopic Mass 243.22
Hydrogen Bond Acceptor Count 2.0
Molecular Weight 243.39
Gi Absorption True
Covalent Unit Count 1.0
Total Atom Stereocenter Count 0.0
Total Bond Stereocenter Count 0.0
Lipinski Rule Of 5 True
Inchi InChI=1S/C14H29NO2/c1-2-3-4-5-6-7-8-9-10-11-14(17)15-12-13-16/h16H,2-13H2,1H3,(H,15,17)
Smiles CCCCCCCCCCCC(=O)NCCO
Np Classifier Biosynthetic Pathway Fatty acids
Defined Bond Stereocenter Count 0.0
Egan Rule True
Np Classifier Superclass Fatty amides

  • 1. Outgoing r'ship FOUND_IN to/from Coriandrum Sativum (Plant) Rel Props:Reference:https://doi.org/10.1080/0972060x.2018.1470943