myxopyronin A

Base Information

Chemical Name:myxopyronin A
CAS No.:88192-98-7
Molecular Formula:C₂₃H₃₁NO₆
Molecular Weight:417.502
Hs Code.:
Mol file:88192-98-7.mol

Synonyms:Carbamicacid, [5-[3-(2,5-dimethyl-1-oxo-2,4-octadienyl)-4-hydroxy-2-oxo-2H-pyran-6-yl]-1-hexenyl]-,methyl ester, [R-(E,E,E)]-; Myxopyronin A

Suppliers and Price of myxopyronin A

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
MYXOPYRONIN A 95.00%
5MG
$ 499.81

Total 4 raw suppliers

Chemical Property of myxopyronin A

Chemical Property:

Vapor Pressure:2.5E-15mmHg at 25°C
Boiling Point:569.2°C at 760 mmHg
PKA:5.14±0.50(Predicted)
Flash Point:298.1°C
PSA：105.42000
Density:1.152g/cm³
LogP:4.99140

Purity/Quality:

99% ^*data from raw suppliers

MYXOPYRONIN A 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of myxopyronin A

There total 12 articles about myxopyronin A 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:

: 10191-25-0
3-oxo-valeric acid

: 88192-98-7
myxopyronin A

Guidance literature:: Multi-step reaction with 8 steps

1: 86 percent / carbonylimidazole / tetrahydrofuran / 18 h

2: 87 percent / n-BuLi, diisopropylamine, HMPA / tetrahydrofuran; hexane / 0.5 h / -78 °C

3: 91 percent / aq. AcOH / tetrahydrofuran / 22 h / Ambient temperature

4: 89 percent / pyridine, Dess-Martin periodinate / CH₂Cl₂ / 2 h / Ambient temperature

5: 82 percent / NaH / tetrahydrofuran / 3 h / Ambient temperature

6: 1.) TiCl₄, DIPEA / 1.) CH₂Cl₂, 2.) CH₂Cl₂

7: 100 percent / aq. LiOH / tetrahydrofuran / Ambient temperature

With pyridine; N,N,N,N,N,N-hexamethylphosphoric triamide; lithium hydroxide; n-butyllithium; carbonylimidazole; titanium tetrachloride; sodium hydride; Dess-Martin periodane; acetic acid; diisopropylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1021/jo9721610

Reference yield:

: 30801-96-8
(E)-3-methylhex-2-en-1-ol

: 88192-98-7
myxopyronin A

Guidance literature:: Multi-step reaction with 4 steps

1: 94 percent / TPAP, NMO / CH₂Cl₂

2: 1.) TiCl₄, DIPEA / 1.) CH₂Cl₂, 2.) CH₂Cl₂

3: 100 percent / aq. LiOH / tetrahydrofuran / Ambient temperature

With lithium hydroxide; N-methyl-2-indolinone; tetrapropylammonium perruthennate; titanium tetrachloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo9721610

Reference yield:

: 38260-16-1
(E)-3-methyl-hex-2-enal

: 88192-98-7
myxopyronin A

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) TiCl₄, DIPEA / 1.) CH₂Cl₂, 2.) CH₂Cl₂

2: 100 percent / aq. LiOH / tetrahydrofuran / Ambient temperature

With lithium hydroxide; titanium tetrachloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran;
DOI:10.1021/jo9721610