Suberosin

Base Information

Chemical Name:Suberosin
CAS No.:581-31-7
Molecular Formula:C15H16O3
Molecular Weight:244.29
Hs Code.:
NSC Number:31869
DSSTox Substance ID:DTXSID20206820
Nikkaji Number:J11.513D
Wikidata:Q27137382
Metabolomics Workbench ID:125570
ChEMBL ID:CHEMBL1928409
Mol file:581-31-7.mol

Synonyms:suberosin

Suppliers and Price of Suberosin

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

Crysdot
Suberosin 95+%
5mg
$ 305.00

ChemScene
Suberosin 99.61%
20mg
$ 514.00

ChemScene
Suberosin 99.61%
5mg
$ 178.00

ChemScene
Suberosin 99.61%
10mg
$ 303.00

Biosynth Carbosynth
Suberosin
25 mg
$ 250.00

Biosynth Carbosynth
Suberosin
10 mg
$ 125.00

Biosynth Carbosynth
Suberosin
5 mg
$ 75.00

Arctom
Suberosin ≥98%
20mg
$ 188.00

Arctom
Suberosin ≥98%
10mg
$ 174.55

AK Scientific
Suberosin
10mg
$ 218.00

Total 27 raw suppliers

Chemical Property of Suberosin

Chemical Property:

Vapor Pressure:2.16E-06mmHg at 25°C
Melting Point:87.5 °C(Solv: methanol (67-56-1))
Refractive Index:1.556
Boiling Point:393.3 °C at 760 mmHg
Flash Point:166 °C
PSA：39.44000
Density:1.126 g/cm³
LogP:3.31030
XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:244.109944368
Heavy Atom Count:18
Complexity:366

Purity/Quality:

99% ^*data from raw suppliers

Suberosin 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)OC)C

Technology Process of Suberosin

There total 1 articles about Suberosin 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: 50.0%

: 73490-50-3
Z-4,5-dimethoxy-2-prenyloxycinnamic acid

: 92-61-5
7-hydroxy-6-methoxy-2H-1-benzopyran-2-one

: 120-08-1
Scoparone

: 581-31-7
suberosin

Guidance literature:: With acetic anhydride; In xylene; at 140 ℃; for 4h;

Reference yield: 89.0%

: 581-31-7
suberosin

: 38409-28-8,80368-68-9
suberosin epoxide

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 0.5h;
DOI:10.1016/S0040-4039(01)01355-7

Reference yield:

: 581-31-7
suberosin

: 74794-82-4
7-methoxy-6-(3'-methyl-4'-phenylbut-2'-enyl)coumarin

Guidance literature:: Multi-step reaction with 3 steps

1: 0.7 g / SeO₂ / acetic acid / 48 h / Heating

2: 0.12 g / K₂CO₃ / methanol / 2 h / Heating

3: 0.06 g / BF₃*Et₂O, 4A molecular sieves / 48 h / Heating

With selenium(IV) oxide; 4 A molecular sieve; boron trifluoride diethyl etherate; potassium carbonate; In methanol; acetic acid;
DOI:10.1071/CH9800395