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N6-Benzyladenine

PubChem CID: 62389

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Compound Synonyms 6-Benzylaminopurine, 1214-39-7, Benzyladenine, N6-Benzyladenine, 6-Benzyladenine, N-Benzyladenine, N-Benzyl-9H-purin-6-amine, 6-(Benzylamino)purine, Benzylaminopurine, Cytokinin B, Adenine, N-benzyl-, N-benzyl-7H-purin-6-amine, 6-BAP, N(6)-Benzylaminopurine, Benzyl(purin-6-yl)amine, 6-(N-Benzylamino)purine, 1H-PURIN-6-AMINE, N-(PHENYLMETHYL)-, Pro-Shear, BA (Growth stimulant), BAP (growth stimulant), N(sup 6)-Benzyladenine, Verdan senescence inhibitor, Aminopurine, 6-benzyl, Caswell No. 081EE, N-Benzyl-adenine, N(sup 6)-(Benzylamino)purine, N-(Phenylmethyl)-1H-purin-6-amine, 6-Benzyl adenine, N-6-Benzyladenine, N(6)-(benzylamino)purine, Adenine, N(sup 6)-benzyl-, Adenine, N6-benzyl-, CCRIS 4351, SD 4901, SQ 4609, ABG 3034, Benzyl Aminopurine, 6-[(phenylmethyl)amino]-9H-purine, EINECS 214-927-5, KXG6A989PS, 6-(Benzylamino)-9H-purine, MFCD00005572, NSC 40818, n(6)-benzyladenine, CYTOPURINE, CHEBI:29022, HSDB 7667, NSC-40818, BENZYLADENINE [MI], BENZYLADENINE, 6-, 9H-Purin-6-amine, N-(phenylmethyl)-, BENZYLADENINE [HSDB], N-benzyl-1H-purin-6-amine, MLS000532693, BAP 99, CHEMBL228862, DTXSID7032630, SMR000140130, CAS-1214-39-7, 6-BA, 6-((phenylmethyl)amino)-9H-purine, benzylpurin-6-ylamine, 6-(n-benzyl)aminopurine, UNII-KXG6A989PS, NBenzyladenine, 6benzyladenine, ProShear, benzyl-(7h-purin-6-yl)-amine, Adenine, Nbenzyl, 6-benzylaminopurin, BAP (cytokinin), Prestwick_414, n6-benzylaminopurine, 6(Benzylamino)purine, Benzyl(purin6yl)amine, 6(NBenzylamino)purine, benzylaminopurine, 6-, N(6)Benzylaminopurine, 6-BA cpd, N(sup 6)Benzyladenine, N-Benzyladenine, 8CI, N(Sup6)-Benzyladenine, BA (growth stimulator), Opera_ID_868, Prestwick0_000189, Prestwick1_000189, Prestwick2_000189, Prestwick3_000189, Adenine, N(sup 6)benzyl, N(Sup 6)-benzyl-Adenine, CBKinase1_000521, CBKinase1_012921, Cambridge id 5131951, TimTec1_001722, BENZYLADENINE [INCI], Oprea1_747691, Oprea1_785203, Oprea1_830563, SCHEMBL35562, BSPBio_000117, CBDivE_001815, N(Phenylmethyl)1Hpurin6amine, MLS001074298, N(sup 6)(Benzylamino)purine, SPBio_002038, 6-Benzylaminopurine, 99.0%, 6-Benzylaminopurine (Standard), BPBio1_000129, 1HPurin6amine, N(phenylmethyl), 9HPurin6amine, N(phenylmethyl), DTXCID5012630, N-benzyladenine, monosodium salt, HY-B0941R, NWBJYWHLCVSVIJ-UHFFFAOYSA-, 6-Benzylaminopurine 100 microg/mL in Acetonitrile/Acetone, HMS1538O06, HMS1568F19, HMS1667I06, HMS2095F19, HMS2234B24, HMS3374C09, HMS3712F19, N-benzyladenine, monopotassium salt, 6-benzyladenine 6-benzylaminopurine, HY-B0941, NSC40818, STR06184, N-(phenylmethyl)-7H-purin-6-amine, Tox21_301307, AC7620, BDBM50205363, CCG-55533, GEO-00296, MFCD00051031, N-(Phenylmethyl)-9H-Purin-6-amine, s4511, STK858495, AKOS002304241, AKOS005257767, 7H-purin-6-amine, N-(phenylmethyl)-, AC-5488, CCG-220189, FB02966, KS-5285, PS-3425, 6-Benzylaminopurine, analytical standard, USEPA/OPP Pesticide Code: 116901, N-benzyl-9H-purin-6-amine, AldrichCPR, NCGC00016571-01, NCGC00016571-02, NCGC00016571-03, NCGC00016571-04, NCGC00016571-05, NCGC00255357-01, SY014632, 6-Benzylaminopurine, >=99.0% (HPLC), B1088, NS00005241, BA, N6-Benzyladenine, N6-Benzyladenine, BA, EN300-40176, 6-Benzylaminopurine, plant cell culture tested, Q419946, SR-01000644553, 6-Benzylaminopurine, Vetec(TM) reagent grade, 98%, SR-01000644553-1, SR-01000644553-2, BA, N6-Benzyladenine, N6-Benzyladenine, BA, BRD-K62929068-001-05-8, BRD-K62929068-001-15-7, BRD-K62929068-001-16-5, Z57245233, 6-Benzylaminopurine, ReagentPlus(R), >=99.0% (HPLC), F0578-0089, 2B76FFBD-3C3A-4349-9047-E5B8945B54A7, ((2r,3s,4r,5r)-5-(4-amino-2-oxopyrimidin-1(2h)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyltriphosph, InChI=1/C12H11N5/c1-2-4-9(5-3-1)6-13-11-10-12(15-7-14-10)17-8-16-11/h1-5,7-8H,6H2,(H2,13,14,15,16,17)
Topological Polar Surface Area 66.5
Hydrogen Bond Donor Count 2.0
Inchi Key NWBJYWHLCVSVIJ-UHFFFAOYSA-N
Rotatable Bond Count 3.0
State Solid
Substituent Name 6-alkylaminopurine, Phenylmethylamine, Benzylamine, Aralkylamine, Secondary aliphatic/aromatic amine, Aminopyrimidine, Imidolactam, Benzenoid, Pyrimidine, Monocyclic benzene moiety, Heteroaromatic compound, Imidazole, Azole, Azacycle, Secondary amine, Hydrocarbon derivative, Organonitrogen compound, Amine, Aromatic heteropolycyclic compound
Synonyms 1H-Purin-6-amine, N-(phenylmethyl)-, 6-(Benzylamino)purine, 6-(N-Benzylamino)purine, 6-[(phenylmethyl)amino]-9H-purine, 6-BAP, 6-Benzyl adenine, 6-Benzyladenine, 6-Benzylaminopurine, 9H-Purin-6-amine, N-(phenylmethyl)-, 9H-Purine, 6-[(phenylmethyl)amino]-, Adenine, n-benzyl-, Adenine, N(sup 6)-benzyl-, Aminopurine, 6-benzyl, BAP, Benzyl(purin-6-yl)amine, Benzyladenine, Benzylaminopurine, Cytokinin B, N-(Phenylmethyl)-1H-purin-6-amine, N-(Phenylmethyl)-9H-purin-6-amine, N-6-Benzyladenine, N-benzyl-1H-purin-6-amine, N-Benzyl-9H-purin-6-amine, N-Benzyl-adenine, N-Benzyladenine, N-Benzyladenine, 8CI, N(6)-(benzylamino)purine, N(6)-Benzylaminopurine, N(sup 6)-(Benzylamino)purine, N(sup 6)-Benzyladenine, N(Sup6)-Benzyladenine, N6-Benzyladenine, 6-[(Phenylmethyl)amino]-9H-purine, Cytokinin b, N-BENZYL-9H-purin-6-amine, N(6)-(Benzylamino)purine, N-Benzyl-1H-purin-6-amine, N(6)-Benzyladenine, 6-BA CPD, 6-Benzylaminopurin, 6-BA, 6-Benzylaminoadenine, BA, N6-(Benzylamino)purine, N6-Benzylaminopurine
Heavy Atom Count 17.0
Compound Name N6-Benzyladenine
Kingdom Organic compounds
Description 6-Benzylaminopurine, benzyl adenine or BAP is a first-generation synthetic cytokinin which elicits plant growth and development responses, setting blossoms and stimulating fruit richness by stimulating cell division. It is an inhibitor of respiratory kinase in plants, and increases post-harvest life of green vegetables. Cytokinin B is found in wild celery and garden tomato (variety).
Exact Mass 225.101
Formal Charge 0.0
Monoisotopic Mass 225.101
Isotope Atom Count 0.0
Molecular Complexity 241.0
Hydrogen Bond Acceptor Count 4.0
Molecular Weight 225.25
Database Name fooddb_chem_all;hmdb_chem_all;pubchem
Covalent Unit Count 1.0
Defined Atom Stereocenter Count 0.0
Iupac Name N-benzyl-7H-purin-6-amine
Total Atom Stereocenter Count 0.0
Molecular Framework Aromatic heteropolycyclic compounds
Total Bond Stereocenter Count 0.0
Class Imidazopyrimidines
Inchi InChI=1S/C12H11N5/c1-2-4-9(5-3-1)6-13-11-10-12(15-7-14-10)17-8-16-11/h1-5,7-8H,6H2,(H2,13,14,15,16,17)
Smiles C1=CC=C(C=C1)CNC2=NC=NC3=C2NC=N3
Xlogp 2.1
Superclass Organoheterocyclic compounds
Defined Bond Stereocenter Count 0.0
Subclass Purines and purine derivatives
Taxonomy Direct Parent 6-alkylaminopurines
Molecular Formula C12H11N5

  • 1. Outgoing r'ship FOUND_IN to/from Apium Graveolens (Plant) Rel Props:Source_db:fooddb_chem_all
  • 2. Outgoing r'ship FOUND_IN to/from Lycopersicon Esculentum (Plant) Rel Props:Source_db:fooddb_chem_all
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