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Catalog Number | ACM27773393 |
CAS Number | 27773-39-3 |
Structure | ![]() |
Synonyms | Ervamycine |
Molecular Weight | 366.5 |
InChI | InChI=1S/C22H26N2O3/c1-4-21-8-5-10-24-11-9-22(20(21)24)16-7-6-14(26-2)12-17(16)23-18(22)15(13-21)19(25)27-3/h5-8,12,20,23H,4,9-11,13H2,1-3H3/t20-,21-,22-/m0/s1 |
InChI Key | AEXBRBWRPNGGEZ-FKBYEOEOSA-N |
Purity | 95%+ |
Complexity | 716 |
Covalently-Bonded Unit Count | 1 |
Defined Atom Stereocenter Count | 3 |
Exact Mass | 366.1943427 |
Heavy Atom Count | 27 |
Hydrogen Bond Acceptor Count | 5 |
Hydrogen Bond Donor Count | 1 |
Isomeric SMILES | CC[C@]12CC(=C3[C@@]4([C@H]1N(CC4)CC=C2)C5=C(N3)C=C(C=C5)OC)C(=O)OC |
Monoisotopic Mass | 366.1943427 |
PhysicalState | Powder |
Rotatable Bond Count | 4 |
Topological Polar Surface Area | 50.8 Ų |
What is the chemical formula of Ervamycine?
The chemical formula of Ervamycine is C22H26N2O3.
What is the CAS number for 16-Methoxytabersonine?
The CAS number for 16-Methoxytabersonine is 27773-39-3.
What is the molecular weight of 16-Methoxytabersonine?
The molecular weight of 16-Methoxytabersonine is 366.46 g/mol.
What is the boiling point of Ervamycine?
The predicted boiling point of Ervamycine is 514.6±50.0 °C.
How is 16-Methoxytabersonine used in synthesis?
16-Methoxytabersonine can be hydrogenated over PtO2 to give the 6:7-dihydro derivative, or heated with 5N-HCl to hydrolyze and decarboxylate to furnish 16-methoxy-1,2-dehydro-aspidospermidine.
What is the melting point of 16-Methoxytabersonine?
The crystalline hydrochloride of 16-Methoxytabersonine has a melting point of 184-6°C (dec.).
How is 16-Methoxytabersonine related to tabersonine?
16-Methoxytabersonine is the 16-methoxy derivative of tabersonine.
What is the specific rotation of the free base form of 16-Methoxytabersonine?
The free base form of 16-Methoxytabersonine has a specific rotation of [α]23D -310° ± 2°.
How is 16-Methoxytabersonine classified in terms of compound type?
16-Methoxytabersonine is classified as a monoterpenoid indole alkaloid, an organic heteropentacyclic compound, a methyl ester, and a tertiary amino compound.
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