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D-(-)-THREO-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL

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
D-(-)-THREO-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL Property
mp : 163-165 °C(lit.)
refractive index : -30.5 ° (C=1, 6mol/L HCl)
storage temp. : −20°C
Safety
Hazard Codes : Xn,T
Risk Statements : 22-36/37/38-45
Safety Statements : 26-45-53
RIDADR : UN 3259 8/PG 3
WGK Germany : 3
RTECS : TY3100000

D-(-)-THREO-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL Chemical Properties,Usage,Production

Chemical Properties
light yellow powder
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.
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.
D-(-)-THREO-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL Preparation Products And Raw materials
Raw materials
Propiophenone
Preparation Products
Potassium heptadecafluoro-1-octanesulfonate
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716-61-0(D-(-)-THREO-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL)Related Search:
BOC-(1R,2R)-(-)-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL FMOC-(1R,2R)-(-)-2-AMINO-1-(4-NITROPHENYL)-1,3-PROPANEDIOL D-THREO-[DICHLOROACETYL-1-14C]-CHLORAMPHENICOL CHLORAMPHENICOL CINNAMATE Chloramphenicol sodium succinate CHLORAMPHENICOL-[RING-3,5-3H] CHLORAMPHENICOL, [3H(G)] D-THREO Eusynthomycin BROMAMPHENICOL CHLORAMPHENICOL (D5) CHLORAMPHENICOL-ALCOHOL LABOTEST-BB LT00452518 Chloramphenicol (1R,2R)-B13 CHLORAMPHENICOL MALEATE CHLORAMPHENICOL, D-THREO-[DICHLOROACETYL-1,2-14C]- CHLORAMPHENICOL 1-O-BETA-D-GALACTOPYRANOSIDE Chloramphenicol palmitate
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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