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CAS No. | 716-61-0 |
Chemical Name: | D-(-)-THREO-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL |
Synonyms: | levoamine;Chloromycin base;L-BASE (AMINODIOL);chloramphenicolbase;CHLORAMPHENICOL-WATER SOLUBLE;D(-)Threo-1-(4-nitro-phenyl)-2;CHLORAMPHENICOL BASE CRYSTALLINE;(1R,2R)-2-AMINO-1-(4-NITROPHENOL)PROPANE-1,3-DIOL;(1R,2R)-2-AMINO-1-(4-NITROPHENYL)PROPANE-1,3-DIOL;D-THREO-(-)-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANE |
CBNumber: | CB6452870 |
Molecular Formula: | C9H12N2O4 |
Formula Weight: | 212.2 |
MOL File: | 716-61-0.mol |
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D-(-)-THREO-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL Property |
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refractive index : |
-30.5 ° (C=1, 6mol/L HCl) |
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D-(-)-THREO-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL Chemical Properties,Usage,Production |
Chemical Properties
light yellow powder |
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Usage
D-threo-(-)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol is an impurity of Chloramphenicol (C325030), a broad spectrum antibiotic agent obtained from cultures of the soil bacterium Streptomyces venezuel
ae. |
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Usage
Chloramphenicol base is the parent 4-nitrophenylpropylamine formed by the hydrolysis of the dichloroacetamide of chloramphenicol and is a degradation product commonly encountered with commercial production of chloramphenicol. Chloramphenicol base has no antibiotic activity but has played an integral role in the synthesis and SAR of new generation antibiotics, notably thiamphenicol and experimental analogues, bromamphenicol and methamphenicol. |
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D-(-)-THREO-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL Suppliers Global( 94)Suppliers |
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d-threo-(-)-2-amino-1-(p-nitrophenyl)-1,3-propanediol
levoamine
Optical Resolution
Chiral Building Blocks
for Resolution of Acids
Amino Alcohols (Chiral)
D-(-)-THREO-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL
D(-)THREO-1-(4-NITRO-PHENYL)-2-AMINO-1,3-PROPANEDIOL
CHLORAMPHENICOL-WATER SOLUBLE
716-61-0
(1R,2R)-2-AMINO-1-(4-NITROPHENOL)PROPANE-1,3-DIOL
(1R,2R)-(-)-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL
(1R,2R)-2-AMINO-1-(4-NITROPHENYL)PROPANE-1,3-DIOL
Amino Alcohols
Asymmetric Synthesis
Organic Building Blocks
D-(-)threo-2-amino-1-(p-nitrophenyl)propane-1,3-diol
AMINE
CHLORAMPHENICOL BASE CRYSTALLINE
(1R,2R)-(-)-2-AMINO-1-ITROPHENYL)-1,3-PR OPANEDIOL,99%
D(-)Threo-1-(4-nitro-phenyl)-2
1,3-Propanediol, 2-amino-1-(4-nitrophenyl)-, (1R,2R)-
D-THREO-(-)-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANE
(1R,2R)-(-)-2-AMINO-1-NITROPHENYL)-1,3-PROPANEDIOL
Amino Alcohols (Chiral)
Chiral Building Blocks
for Resolution of Acids
Optical Resolution
Synthetic Organic Chemistry
Chloromycin base
Antibiotics
Cell Culture
Reagents and Supplements
Chloramphenicol base, D-(-)-threo-2-Amino-1-(p-nitrophenyl)-1,3-propanediol
HOCH2CHNH2CHC6H4NO2OH
2-amino-1-(p-nitrophenyl)-3-propanediod-threo-(-)-
chloramphenicolbase
(1R,2R)-1-(4-Nitrophenyl)-2-aminopropane-1,3-diol
[1R,2R,(-)]-2-Amino-1-(p-nitrophenyl)-1,3-propanediol
(1R,2R)-2-Amino-1-(4-nitrophenyl)propane-1,3-diol,96%
C9H12O4N2
(1R,2R)-()-2-Amino-1-(4-nitrophenyl)-1,3-propanediol,D-()-threo-2-Amino-1-(p-nitrophenyl)-1,3-propanediol, Chloramphenicol base
(1R,2R)-2-AMino-1-(4-nitrophenyl)propane-1,3-diol, 96% 5GR
L-BASE (AMINODIOL)
(1R,2R)-(-)-2-AMino-1-(4-nitrophenyl)-1,3-propanediol 99%
(1R,2R)-(-)-2-AMino-1-(4-nitrophenyl)-1,3-propanediol, 96%, 96%
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