Zamamistatin

Base Information

Chemical Name:Zamamistatin
CAS No.:30951-40-7
Molecular Formula:C₉H₉Br₂NO₃
Molecular Weight:338.983
Hs Code.:
Nikkaji Number:J329.222C
Wikidata:Q104935791
Metabolomics Workbench ID:167073
Mol file:30951-40-7.mol

Synonyms:Zamamistatin;(-)-Aeroplysinin I;(-)-Aeroplysinin 1;AEROPLYSININ-I (RACEMIC);55057-73-3;30951-40-7;(-)3,5-Dibromo-1(ax),6(ax)dihydroxy-4-methoxycyclohexa-2,4-diene-1-acetonitrile

Suppliers and Price of Zamamistatin

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

Total 0 raw suppliers

Chemical Property of Zamamistatin

Chemical Property:

Vapor Pressure:3.27E-11mmHg at 25°C
Boiling Point:479.6°C at 760 mmHg
Flash Point:243.8°C
Density:2.01g/cm³
XLogP3:0.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:338.89287
Heavy Atom Count:15
Complexity:382

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C(C(C=C1Br)(CC#N)O)O)Br
Isomeric SMILES:COC1=C([C@H]([C@](C=C1Br)(CC#N)O)O)Br

Technology Process of Zamamistatin

There total 5 articles about Zamamistatin 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: 96.0%

: 876301-52-9
(5R,10S)-methyl 7,9-dibromo-10-hydroxy-8-methoxy-1-oxa-2-azaspiro[4.5]deca-2,6,8-triene-3-carboxylate

: 30951-40-7
(-)-aeroplysinin-1

Guidance literature:: With sodium hydroxide; Heating;
DOI:10.1016/j.tetlet.2005.11.097

Reference yield:

: 876301-49-4
(5R,10S)-7,9-Dibromo-8-methoxy-10-((1S,4R)-4,7,7-trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carbonyloxy)-1-oxa-2-aza-spiro[4.5]deca-2,6,8-triene-3-carboxylic acid methyl ester

: 30951-40-7
(-)-aeroplysinin-1

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / K₂CO₃ / methanol

2: 96 percent / aq.NaOH / Heating

With sodium hydroxide; potassium carbonate; In methanol;
DOI:10.1016/j.tetlet.2005.11.097

Reference yield:

: 87580-09-4,87580-10-7
(5S*,6R*)-methyl 7,9-dibromo-8-methoxy-6-oxo-1-oxa-2-azaspiro<4.5>deca-2,7,9-triene-3-carboxylate

: 30951-40-7
(-)-aeroplysinin-1

Guidance literature:: Multi-step reaction with 3 steps

1: 47 percent / pyridine / CH₂Cl₂

2: 100 percent / K₂CO₃ / methanol

3: 96 percent / aq.NaOH / Heating

With pyridine; sodium hydroxide; potassium carbonate; In methanol; dichloromethane;
DOI:10.1016/j.tetlet.2005.11.097