Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C29H46Cl2N2O6 |
| Molecular Weight | 589.591 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](NC(=O)C(Cl)Cl)[C@H](O)C1=CC=C(C=C1)[N+]([O-])=O
InChI
InChIKey=IDWDXHQLOMJDRU-XNMGPUDCSA-N
InChI=1S/C29H46Cl2N2O6/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-26(34)39-22-25(32-29(36)28(30)31)27(35)23-18-20-24(21-19-23)33(37)38/h18-21,25,27-28,35H,2-17,22H2,1H3,(H,32,36)/t25-,27-/m1/s1
| Molecular Formula | C29H46Cl2N2O6 |
| Molecular Weight | 589.591 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Surface area and crystallinity of Form A of chloramphenicol palmitic and stearic esters: which one is the limiting factor in the enzymatic hydrolysis? | 1987-12 |
|
| [Pseudomorphism of chloramphenicol stearate and palmitate in relationship availability]. | 1983-04 |
|
| [Effect of surfactants on the in vitro enzymatic hydrolysis of chloramphenicol stearate]. | 1981-06 |
|
| [Determination of the crystallinity of biologically active polymorph forms of chloramphenicol stearate: correlation with in vitro enzymatic hydrolysis]. | 1979-08 |
|
| Polymorphism of chloramphenicol stearate. II - Kinetics of solid-state transition of crystal forms. | 1978-10 |
|
| [Polymorphism of chloramphenicol stearate]. | 1978 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:54:40 GMT 2025
by
admin
on
Mon Mar 31 20:54:40 GMT 2025
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| Record UNII |
DL2A9M9D6X
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| Record Status |
Validated (UNII)
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| Record Version |
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