Citromycetin

Base Information

Chemical Name:Citromycetin
CAS No.:478-60-4
Molecular Formula:C₁₄H₁₀O₇
Molecular Weight:290.229
Hs Code.:
NSC Number:53584
UNII:6LQ9JP1YA7
DSSTox Substance ID:DTXSID60197283
Nikkaji Number:J6.149B
Wikipedia:Citromycetin
Wikidata:Q15410873
Mol file:478-60-4.mol

Synonyms:citromycetin

Suppliers and Price of Citromycetin

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
Citromycetin
1mg
$ 310.00

Cayman Chemical
Citromycetin ≥95%
5mg
$ 1282.00

Cayman Chemical
Citromycetin ≥95%
1mg
$ 302.00

Biosynth Carbosynth
Citromycetin
1 mg
$ 190.00

Biosynth Carbosynth
Citromycetin
0.5 mg
$ 100.00

Biosynth Carbosynth
Citromycetin
5 mg
$ 450.00

Biosynth Carbosynth
Citromycetin
2 mg
$ 340.00

Biosynth Carbosynth
Citromycetin
10 mg
$ 840.00

American Custom Chemicals Corporation
CITROMYCETIN 95.00%
5MG
$ 499.00

AK Scientific
Citromycetin
10mg
$ 1184.00

Total 11 raw suppliers

Chemical Property of Citromycetin

Chemical Property:

Vapor Pressure:8.16E-19mmHg at 25°C
Boiling Point:669.1°Cat760mmHg
Flash Point:260.9°C
PSA：117.20000
Density:1.73g/cm³
LogP:1.61700
XLogP3:1.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:1
Exact Mass:290.04265265
Heavy Atom Count:21
Complexity:562

Purity/Quality:

99% ^*data from raw suppliers

Citromycetin ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=O)C2=C(O1)C3=C(C=C(C(=C3C(=O)O)O)O)OC2
Uses Citromycetin was independently isolated and named from a number of different fungal species during the 1930s to 1950s and subsequently shown to be identical. Citromycetin is active against Gram positive bacteria. NCI studies demonstrated the lack of activity against tumours and AIDS. Citromycetin is an interesting metabolite which has received little attention in modern times. Citromycetin is an antibacterial reagent active against Gram positive bacteria.

Technology Process of Citromycetin

There total 9 articles about Citromycetin 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: 69.0%

: 101905-34-4
O,O-dimethylcitromycetin

: 478-60-4
Citromycetin

Guidance literature:: With aluminium trichloride; dimethylsulfide; In dichloromethane; for 15h; Ambient temperature;
DOI:10.1039/P19870000395

Reference yield: 64.0%

: 478-60-4
Citromycetin

Guidance literature:: With hydrogenchloride; In methanol; for 240h; Ambient temperature;
DOI:10.1039/P19880000763

Reference yield:

: 101905-32-2
8,9-dimethoxy-2-methyl-10-(prop-1-enyl)pyrano<3,2-c><1>-benzopyran-4(5H)-one

: 478-60-4
Citromycetin

Guidance literature:: Multi-step reaction with 3 steps

1: O₃, Oil Violet

2: sodium chlorite, sulphamic acid

3: 69 percent / AlCl₃, Me₂S / CH₂Cl₂

With sodium chlorite; aluminium trichloride; dimethylsulfide; oil violet; aminosulfonic acid; ozone; In dichloromethane;
DOI:10.1039/c39850001483