(1R,2R)-(-)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol CAS 716-61-0 Purity ≥99.0% (HPLC) High Purity

Short Description:

Name: (1R,2R)-(-)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol 

D-(-)-threo-2-Amino-1-(4-nitrophenyl)-1,3-propanediol

CAS: 716-61-0

Appearance: White to Pale Yellow Powder

Purity: ≥99.0% (HPLC)

Chiral Compounds, Commercial Production

E-mail: alvin@ruifuchem.com


Product Detail

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Description:

Chemical Properties:

Chemical Name (1R,2R)-(-)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol 
Synonyms D-(-)-threo-2-Amino-1-(4-nitrophenyl)-1,3-propanediol; Chloramphenico L-Base;  L-Base; Levoamine
CAS Number 716-61-0
CAT Number RF-CC292
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C9H12N2O4
Molecular Weight 212.2
Solubility Soluble in Water, Ethanol, Methanol, DMF, DMSO
Shipping Condition Shipped Under Ambient Temperature
Brand Ruifu Chemical

Specifications:

Item Specifications
Appearance White to Pale Yellow Powder 
Melting Point 160.0~165.0℃
Loss on Drying ≤0.50%
Residue on Ignition ≤0.50%
Optical Rotation [a]20D -28.5° ~ -30.5° 
Moisture (K.F) ≤0.50%
Purity / Analysis Method ≥99.0% (HPLC)
Single Impurity ≤0.50%
Total Impurities ≤1.0%
Test Standard Enterprise Standard
Usage Pharmaceutical Intermediates; Chloramphenico L-Base

Package & Storage:

Package: Bottle, Aluminium foil bag, Cardboard Drum, 25kg/Drum, or according to customer's requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.

Advantages:

1

FAQ:

Application:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of (1R,2R)-(-)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol (CAS: 57794-08-8), also named D-(-)-threo-2-Amino-1-(4-nitrophenyl)-1,3-propanediol with high quality.

(1R,2R)-(-)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol (CAS: 57794-08-8) (Chloramphenicol base) is an intermediate for synthesizing Chloramphenicol, a broad spectrum antibiotic agent. Chloramphenicol base is the parent 4-nitrophenylpropylamine formed by the hydrolysis of the dichloroacetamide of chloramphenicol. Chloramphenicol base per se does not work as an antibiotic, however, it plays an important role in the synthesis and antibacterial activities of chloramphenicol and other new generation antibiotics, represented by thiamphenicol and its experimental analogues, bromamphenicol and methamphenicol.

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