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Basic Information
CAS No.: 12728-25-5
Name: Desertomycin
Molecular Structure:
Molecular Structure of 12728-25-5 (Desertomycin)
Formula: C61H109NO21
Molecular Weight: 1192.51226
Synonyms: desertomycin
Density: 1.28g/cm3
Boiling Point: 1269.6°Cat760mmHg
Flash Point: 721.6°C
Safety: Poison by ingestion, intraperitoneal, subcutaneous, and intravenous routes.
PSA: 414.69000
LogP: 1.14270
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Chemistry

IUPAC  Name: 41-(6-Amino-3-hydroxyhexan-2-yl)-7,9,15,19,23,25,27,29,31,33,35,37-dodecahydroxy-2,6,8,14,18,20,30,32-octamethyl-22-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-42-oxacyclodotetraconta-2,12,16,20,38-pentaen-1-one    
Molecular Formula: C61H109NO21
Molecular Weight: 1192.51
Freely Rotating Bonds: 26
Polar Surface Area: 204.91 Å2
Index of Refraction: 1.59
Molar Refractivity: 313.98 cm3
Molar Volume: 929.3 cm3
Polarizability: 124.47 ×10-24 cm3
Surface Tension: 68.7 dyne/cm
Density: 1.28 g/cm3
Flash Point: 721.6 °C
Enthalpy of Vaporization: 213.91 kJ/mol
Boiling Point: 1269.6 °C at 760 mmHg
Vapour Pressure: 0 mmHg at 25°C 
The Cas Register Number of  Desertomycin is 12728-25-5. The chemical synonyms of  Desertomycin (CAS NO.12728-25-5) are 41-(6-Amino-3-hydroxyhexan-2-yl)-7,9,15,19,23,25,27,29,31,33,35,37-dodecahydroxy-2,6,8,14,18,20,30,32-octamethyl-22-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-42-oxacyclodotetraconta-2,12,16,20,38-pentaen-1-one .The molecular structure of  Desertomycin (CAS NO.12728-25-5) is.

Uses

 Desertomycin (CAS NO.12728-25-5) is used in organic synthesis .

Toxicity Data With Reference

1.    

orl-mus LD50:12,000 µg/kg

     85ERAY    Antibiotics: Origin, Nature, and Properties. 2 (1978),1367.
2.    

ipr-mus LD50:2600 µg/kg

     85ERAY    Antibiotics: Origin, Nature, and Properties. 2 (1978),1367.
3.    

scu-mus LD50:5300 µg/kg

     85ERAY    Antibiotics: Origin, Nature, and Properties. 2 (1978),1367.
4.    

ivn-mus LD50:1350 µg/kg

     85ERAY    Antibiotics: Origin, Nature, and Properties. 2 (1978),1367.

Safety Profile

Poison by ingestion, intraperitoneal, subcutaneous, and intravenous routes.