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N6-Benzoyladenine - ≥98.0%(HPLC), high purity , CAS No.4005-49-6
Basic Description Synonyms BDBM85771 | N-(9H-purin-6-yl)benzamide, AldrichCPR | N-(9H-Purin-6-yl)benzamide # | MFCD00037927 | N4-Benzoyladenine | N6-Benzoyladenine, >=99% | ADENINE, N6-BENZOYL- | STL220128 | AC-32453 | CS-W014659 | O11997 | 6-Benzamidopurine | 7BQB2WI1II | N-[3-[7- Specifications & Purity ≥98%(HPLC) Storage Temp Store at 2-8°C Shipped In Wet ice Product Description It is used in the organic synthesis of adenine derivative molecules such as bicyclic adenine nucleoside via a condensation reaction between L-threo-pentofuranose derivative 1 and 6-N-benzoyladenine and to produce oxy-peptide nucleic acids.
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Names and Identifiers Pubchem Sid 504756352 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504756352 IUPAC Name N-(7H-purin-6-yl)benzamide INCHI InChI=1S/C12H9N5O/c18-12(8-4-2-1-3-5-8)17-11-9-10(14-6-13-9)15-7-16-11/h1-7H,(H2,13,14,15,16,17,18) InChi Key QQJXZVKXNSFHRI-UHFFFAOYSA-N Canonical SMILES C1=CC=C(C=C1)C(=O)NC2=NC=NC3=C2NC=N3 Isomeric SMILES C1=CC=C(C=C1)C(=O)NC2=NC=NC3=C2NC=N3 PubChem CID 97075 Molecular Weight 239.24 Beilstein 26(4)3583 Reaxy-Rn 20585
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