APO-beta-ERYTHROIDINE

Base Information

Chemical Name:APO-beta-ERYTHROIDINE
CAS No.:478-85-3
Molecular Formula:C15H15NO2
Molecular Weight:241.2851
Hs Code.:
UNII:F1KCY9Q2FQ
DSSTox Substance ID:DTXSID60197288
Wikidata:Q27277519
Mol file:478-85-3.mol

Synonyms:APO-beta-ERYTHROIDINE;BRN 0252154;UNII-F1KCY9Q2FQ;F1KCY9Q2FQ;478-85-3;11H-Pyrano(3,4-d)pyrrolo(3,2,1-jk)(1)benzazepin-11-one, 4,5,7,8,9,12-hexahydro-;4-27-00-02889 (Beilstein Handbook Reference);APO-.BETA.-ERYTHROIDINE;DTXSID60197288;APO-.BETA.-ERYTHROIDINE [MI];LS-21456;Q27277519;4,5,7,8,9,12-Hexahydro-5H-pyrano[3,4-d]pyrrolo[3,2,1-jk][1]benzazepin-5-one;5H-PYRANO(3,4-D)PYRROLO(3,2,1-JK)(1)BENZAZEPIN-5-ONE, 4,7,8,9,11,12-HEXAHYDRO-

Suppliers and Price of APO-beta-ERYTHROIDINE

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
APO-BETA-ERYTHROIDINE 95.00%
5MG
$ 496.18

Total 0 raw suppliers

Chemical Property of APO-beta-ERYTHROIDINE

Chemical Property:

Vapor Pressure:4.47E-10mmHg at 25°C
Melting Point:128-129°; mp 132-132.5°
Boiling Point:498.6°C at 760 mmHg
Flash Point:206.7°C
PSA：29.54000
Density:1.31g/cm³
LogP:2.21830
XLogP3:1.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:241.110278721
Heavy Atom Count:18
Complexity:415

Purity/Quality:: APO-BETA-ERYTHROIDINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN2CCC3=C2C(=CC=C3)C4=C1COC(=O)C4

Technology Process of APO-beta-ERYTHROIDINE

There total 4 articles about APO-beta-ERYTHROIDINE 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:

: 2702-45-6
(6-oxo-1,2,5,6-tetrahydro-4H-azepino[3,2,1-hi]indol-7-ylidene)-acetic acid tert-butyl ester

: 478-85-3
4,5,7,8,9,12-hexahydro-pyrano[4',3':4,5]azepino[3,2,1-hi]indol-11-one

Guidance literature:: Multi-step reaction with 2 steps

1: (i) NaH, DMSO, (ii) /BRN= 5390252/

2: H₂ / Pd-BaSO₄ / ethyl acetate / 0.92 h / Ambient temperature

With hydrogen; palladium on barium sulfate; In ethyl acetate;
DOI:10.1021/ja00969a030

Reference yield:

: 2581-08-0
4,5,7,9-tetrahydro-pyrano[4',3':4,5]azepino[3,2,1-hi]indol-11-one

: 478-85-3
4,5,7,8,9,12-hexahydro-pyrano[4',3':4,5]azepino[3,2,1-hi]indol-11-one

: 2581-07-9
4,5,7,8,8a,9-hexahydro-pyrano[4',3':4,5]azepino[3,2,1-hi]indol-11-one

Guidance literature:: With hydrogen; palladium on barium sulfate; In ethyl acetate; for 0.916667h; Ambient temperature;
DOI:10.1021/ja00969a030