Mucidin

Base Information

Chemical Name:Mucidin
CAS No.:52110-55-1
Molecular Formula:C16H18 O3
Molecular Weight:258.317
Hs Code.:2918990090
UNII:15143I0275
DSSTox Substance ID:DTXSID401025570
Nikkaji Number:J9.782I
Wikidata:Q27147658
Metabolomics Workbench ID:98164
Mol file:52110-55-1.mol

Synonyms:Mucidermin;mucidin;strobilurin A

Suppliers and Price of Mucidin

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

TRC
Mucidin
2.5mg
$ 150.00

TRC
Mucidin
25mg
$ 1200.00

American Custom Chemicals Corporation
MUCIDIN 95.00%
5MG
$ 505.98

Total 16 raw suppliers

Chemical Property of Mucidin

Chemical Property:

Vapor Pressure:4.52E-07mmHg at 25°C
Boiling Point:414.2°C at 760 mmHg
Flash Point:175.9°C
PSA：35.53000
Density:1.064g/cm³
LogP:3.34940
XLogP3:3.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:258.125594432
Heavy Atom Count:19
Complexity:372

Purity/Quality:

99% ^*data from raw suppliers

Mucidin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CC=CC1=CC=CC=C1)C(=COC)C(=O)OC
Isomeric SMILES:C/C(=C/C=C/C1=CC=CC=C1)/C(=C\OC)/C(=O)OC
Uses Mucidin (Strobilurin A) is an antifungal antibiotic.

Technology Process of Mucidin

There total 35 articles about Mucidin 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: 85.0%

: 81436-40-0
(9E)-Strobilurin A

: 52110-55-1
methyl (2E,3Z,5E)-2-(methoxymethylene)-3-methyl-6-phenylhexa-3,5-dienoate

Guidance literature:: In acetone; benzene; for 1h; Irradiation;
DOI:10.1002/jlac.198419840910

Reference yield: 79.0%

: 4,4,5,5-tetramethyl-2-((2E,4E)-5-phenylpenta-2,4-dien-2-yl)-1,3,2-dioxaborolane

: methyl (Z)-3-methoxy-2-(((trifluoromethyl)sulfonyl)oxy)acrylate

: 52110-55-1
methyl (2E,3Z,5E)-2-(methoxymethylene)-3-methyl-6-phenylhexa-3,5-dienoate

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate; In water; isopropyl alcohol; for 2h; Reflux; Inert atmosphere;
DOI:10.1002/adsc.201700879

Reference yield:

: 1449-46-3
benzyltriphenylphosphonium bromide

: 52110-55-1
methyl (2E,3Z,5E)-2-(methoxymethylene)-3-methyl-6-phenylhexa-3,5-dienoate

Guidance literature:: Multi-step reaction with 7 steps

1: t-BuOK / tetrahydrofuran / Ambient temperature

2: tetrahydrofuran / Ambient temperature

3: H₂O / pTSA / acetone / 50 °C

4: toluene / Heating

6: NaH / Ambient temperature

7: K₂CO₃ / dimethylformamide / Ambient temperature

With potassium tert-butylate; water; sodium hydride; potassium carbonate; toluene-4-sulfonic acid; In tetrahydrofuran; N,N-dimethyl-formamide; acetone; toluene;
DOI:10.1016/S0040-4039(01)80582-7