CID 20407245

Base Information

Chemical Name:CID 20407245
CAS No.:3922-90-5
Molecular Formula:C₃₅H₆₁NO₁₂
Molecular Weight:687.869
Hs Code.:
European Community (EC) Number:223-495-7
Metabolomics Workbench ID:21280
NCI Thesaurus Code:C61864
Wikipedia:Oleandomycin
Mol file:3922-90-5.mol

Synonyms:Oleandomycin;Oleandomycin Phosphate;Phosphate, Oleandomycin

Suppliers and Price of CID 20407245

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

Usbiological
Oleandomycin
1mg
$ 744.00

TRC
Oleandomycin
1mg
$ 140.00

TRC
Oleandomycin
2.5mg
$ 305.00

Medical Isotopes, Inc.
Oleandomycin
25 NULL
$ 790.00

Medical Isotopes, Inc.
Oleandomycin
10 NULL
$ 650.00

ChemScene
Oleandomycin
10mg
$ 380.00

ChemScene
Oleandomycin
5mg
$ 220.00

Cayman Chemical
Oleandomycin ≥95%
5mg
$ 99.00

Cayman Chemical
Oleandomycin ≥95%
25mg
$ 347.00

ApexBio Technology
Oleandomycin
25mg
$ 432.00

Total 18 raw suppliers

Chemical Property of CID 20407245

Chemical Property:

Vapor Pressure:8.49E-30mmHg at 25°C
Melting Point:110 °C (decomp)
Boiling Point:802.6°C at 760 mmHg
PKA:pKa 8.84(H2O,t =25,I=0.167) (Uncertain)
Flash Point:439.2°C
PSA：165.98000
Density:1.21g/cm³
LogP:1.90850
Storage Temp.:-20°C Freezer
Solubility.:DMSO (Slightly), Methanol (Slightly)
XLogP3:2.6
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:13
Rotatable Bond Count:6
Exact Mass:687.41937638
Heavy Atom Count:48
Complexity:1090

Purity/Quality:

99%, ^*data from raw suppliers

Oleandomycin ^*data from reagent suppliers

Safty Information:

Pictogram(s): Low toxicity by ingestion.
Hazard Codes:Low toxicity by ingestion.

MSDS Files:

Useful:

Canonical SMILES:CC1CC(C(C(O1)OC2C(CC3(CO3)C(=O)C(C(C(C(OC(=O)C(C(C2C)OC4CC(C(C(O4)C)O)OC)C)C)C)O)C)C)O)N(C)C
Isomeric SMILES:C[C@@H]1C[C@@H]([C@H]([C@@H](O1)O[C@H]2[C@@H](C[C@@]3(CO3)C(=O)[C@@H]([C@H]([C@H]([C@H](OC(=O)[C@@H]([C@H]([C@@H]2C)O[C@H]4C[C@@H]([C@H]([C@@H](O4)C)O)OC)C)C)C)O)C)C)O)N(C)C
Uses Antibiotic substance produced by Streptomyces antibioticus no. ATCC 11891. Antibacterial. Oleandomycin is a 16-membered macrocyclic lactone, discovered in the 1950s, with broad spectrum antibacterial activity. Oleandomycin was developed as a human pharmaceutical but was regarded as less active than comparable products such as erythromycin and is today only available in combination with other antibiotics.
Therapeutic Function Antibiotic

Technology Process of CID 20407245

There total 9 articles about CID 20407245 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:

: 119870-69-8
C₂₇H₃₉BrO₇

: 3922-90-5,7562-59-6
oleandomycin

Guidance literature:: Multi-step reaction with 4 steps

1: pyridinium dichromate / CH₂Cl₂ / 8 h / Ambient temperature

2: H₂ / 20percent Pd(OH)2-C / dioxane / 1 h / Ambient temperature

3: 42 percent / silver triflate, MS 4A / toluene; CH₂Cl₂ / 5 h / Ambient temperature

With dipyridinium dichromate; hydrogen; silver trifluoromethanesulfonate; palladium hydroxide - carbon; In 1,4-dioxane; dichloromethane; toluene;
DOI:10.1016/S0040-4039(00)80397-4

Reference yield:

: 119887-69-3
(1S,2R,5R,6R,7R,8R,9R,12S,13S,17R)-15-(4-Bromo-phenyl)-7,9-dihydroxy-2,5,6,8,12,17-hexamethyl-10-methylene-4,14,16-trioxa-bicyclo[11.3.1]heptadecan-3-one

: 3922-90-5,7562-59-6
oleandomycin

Guidance literature:: Multi-step reaction with 5 steps

1: m-chloroperbenzoic acid / CCl₄ / 2 h / Ambient temperature

2: pyridinium dichromate / CH₂Cl₂ / 8 h / Ambient temperature

3: H₂ / 20percent Pd(OH)2-C / dioxane / 1 h / Ambient temperature

4: 42 percent / silver triflate, MS 4A / toluene; CH₂Cl₂ / 5 h / Ambient temperature

With dipyridinium dichromate; hydrogen; silver trifluoromethanesulfonate; 3-chloro-benzenecarboperoxoic acid; palladium hydroxide - carbon; In 1,4-dioxane; tetrachloromethane; dichloromethane; toluene;
DOI:10.1016/S0040-4039(00)80397-4

Reference yield:

: 119870-70-1
C₂₇H₃₇BrO₇

: 3922-90-5,7562-59-6
oleandomycin

Guidance literature:: Multi-step reaction with 3 steps

1: H₂ / 20percent Pd(OH)2-C / dioxane / 1 h / Ambient temperature

2: 42 percent / silver triflate, MS 4A / toluene; CH₂Cl₂ / 5 h / Ambient temperature

With hydrogen; silver trifluoromethanesulfonate; palladium hydroxide - carbon; In 1,4-dioxane; dichloromethane; toluene;
DOI:10.1016/S0040-4039(00)80397-4