Erythromycin C

Base Information

• Chemical Name: Erythromycin C
• CAS No.: 1675-02-1
• Molecular Formula: C36H65 N O13
• Molecular Weight: 719.911
• European Community (EC) Number: 688-004-4
• UNII: 9X2R375YNZ
• Nikkaji Number: J15.156D
• Wikidata: Q27133183
• Metabolomics Workbench ID: 63294
• Mol file: 1675-02-1.mol

Synonyms:Erycette;Erymax;Erythromycin;Erythromycin A;Erythromycin C;Erythromycin Lactate;Erythromycin Phosphate;Ilotycin;Lactate, Erythromycin;Phosphate, Erythromycin;T Stat;T-Stat;TStat

Chemical Property of Erythromycin C

Chemical Property:

• Vapor Pressure: 1.17E-31mmHg at 25°C
• Melting Point: 121-125 °C
• Boiling Point: 826.2°C at 760 mmHg
• PKA: 13.09±0.70(Predicted)
• Flash Point: 453.5°C
• PSA: 204.91000
• Density: 1.23g/cm³
• LogP: 1.13150
• XLogP3: 2.2
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 14
• Rotatable Bond Count: 6
• Exact Mass: 719.44559113
• Heavy Atom Count: 50
• Complexity: 1160

Purity/Quality:

98%Min ^*data from raw suppliers

Erythromycin C ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)O)C)OC3C(C(CC(O3)C)N(C)C)O)(C)O)C)C)O)(C)O
• Isomeric SMILES: CC[C@@H]1[C@@]([C@@H]([C@H](C(=O)[C@@H](C[C@@]([C@@H]([C@H]([C@@H]([C@H](C(=O)O1)C)O[C@H]2C[C@@]([C@H]([C@@H](O2)C)O)(C)O)C)O[C@H]3[C@@H]([C@H](C[C@H](O3)C)N(C)C)O)(C)O)C)C)O)(C)O
• Description: Erythromycin C is an intermediate in the biosynthesis of erythromycin . It is also a potential impurity found in commercial preparations of erythromycin. Erythromycin C is half as active or less than erythromycin A or B against most Gram-positive and Gram-negative bacteria tested.
• Uses: Erythromycin (E649950) impurity. A related substance in Erythromycin drug. Erythromycin C (3’’-O-demethylerythromycin A) is a minor co-metabolite of erythromycin produced by Saccharopolyspora erythreae. Erythromycin C exhibits a narrower spectrum of antibiotic activity and is much less active than erythromycins A and B.

Technology Process of Erythromycin C

There total 1 articles about Erythromycin C 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:

→ erythromycin C (1675-02-1)

Guidance literature:

Reference yield:

erythromycin C (1675-02-1) → erythralosamine (546-57-6,34379-06-1)

Guidance literature:

With methanol; acetyl chloride;

DOI:10.1021/ja01579a060

Downstream raw materials:

erythralosamine

Refernces

• 1、 -. "Erythromycin A 11,12-carbonates and method of use". . . Retrieved 2008/06/13.