(13)Cytochalasa-13,17,21-triene-1,20,23-trione, 19-(acetyloxy)-6,7-epoxy-10-(1H-indol-3-yl)-16,18-dimethyl-

Base Information

Chemical Name:(13)Cytochalasa-13,17,21-triene-1,20,23-trione, 19-(acetyloxy)-6,7-epoxy-10-(1H-indol-3-yl)-16,18-dimethyl-
CAS No.:55653-51-5
Molecular Formula:C34H38N2O6
Molecular Weight:570.6753
Hs Code.:

Synonyms:(13)Cytochalasa-13,17,21-triene-1,20,23-trione, 19-(acetyloxy)-6,7-epoxy-10-(1H-indol-3-yl)-16,18-dimethyl-;19-(Acetyloxy)-6,7-epoxy-10-(1H-indol-3-yl)-16,18-dimethyl-(13)cytochalasa-13,17,21-triene-1,20,23-trione;55653-51-5;[13]Cytochalasa-13,17,21-triene-1,20,23-trione, 19-(acetyloxy)-6,7-epoxy-10-(1H-indol-3-yl)-16,18-dimethyl-

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Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (13)Cytochalasa-13,17,21-triene-1,20,23-trione, 19-(acetyloxy)-6,7-epoxy-10-(1H-indol-3-yl)-16,18-dimethyl-

Chemical Property:

Vapor Pressure:2.31E-24mmHg at 25°C
Boiling Point:781.3°C at 760 mmHg
Flash Point:426.3°C
Density:1.29g/cm³
XLogP3:4.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:570.27298694
Heavy Atom Count:42
Complexity:1250

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CC=CC2C3C(O3)(C(C4C2(C(=O)C=CC(=O)C(C(=C1)C)OC(=O)C)C(=O)NC4CC5=CNC6=CC=CC=C65)C)C
Isomeric SMILES:C[C@H]/1C/C=C/[C@H]2[C@H]3[C@](O3)([C@H]([C@@H]4[C@@]2(C(=O)/C=C/C(=O)[C@@H](/C(=C1)/C)OC(=O)C)C(=O)NC4CC5=CNC6=CC=CC=C65)C)C

Technology Process of (13)Cytochalasa-13,17,21-triene-1,20,23-trione, 19-(acetyloxy)-6,7-epoxy-10-(1H-indol-3-yl)-16,18-dimethyl-

There total 2 articles about (13)Cytochalasa-13,17,21-triene-1,20,23-trione, 19-(acetyloxy)-6,7-epoxy-10-(1H-indol-3-yl)-16,18-dimethyl- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 108-24-7
acetic anhydride

: 50335-03-0
(7S,13E,16S,17E,19R,21E)-6,7-epoxy-19-hydroxy-10-(1H-indol-3-yl)-16,18-dimethyl-<13>cytochalasa-13,17,21-triene-1,20,23-trione, (chaetoglobosin A)

: 50416-39-2
7,19-di-O-acetylchaetoglobosin B

: 50939-69-0,55653-51-5
19-O-acetylchaetoglobosin A

Guidance literature:: In pyridine; Ambient temperature;
DOI:10.1248/cpb.30.1618

Reference yield:

: 108-24-7
acetic anhydride

: (13E,17E,21E)-6,7β-epoxy-19β-hydroxy-10-indol-3-yl-16α,18-dimethyl-[13]cytochalasa-13,17,21-triene-1,20,23-trione

: 50939-69-0,55653-51-5
(13E,17E,21E)-19β-acetoxy-6,7β-epoxy-10-indol-3-yl-16α,18-dimethyl-[13]cytochalasa-13,17,21-triene-1,20,23-trione

Guidance literature:: DOI:10.1016/S0040-4039(01)86820-9

Reference yield:

: 50939-69-0,55653-51-5
19-O-acetylchaetoglobosin A

: 50416-39-2
7,19-di-O-acetylchaetoglobosin B

Guidance literature:: Multi-step reaction with 2 steps

1: 164 mg / HCl (gas) / CHCl₃ / 5 h / Ambient temperature

2: 55 mg / pyridine / 16 h / Ambient temperature

With pyridine; hydrogenchloride; In chloroform;
DOI:10.1002/hlca.19810640710