1-(p-nitrophenyl)-2-amino-1,3-propanediol

Modify Date: 2025-08-26 13:10:19

1-(p-nitrophenyl)-2-amino-1,3-propanediol Structure
1-(p-nitrophenyl)-2-amino-1,3-propanediol structure
Common Name 1-(p-nitrophenyl)-2-amino-1,3-propanediol
CAS Number 2964-48-9 Molecular Weight 212.203
Density 1.4±0.1 g/cm3 Boiling Point 451.9±45.0 °C at 760 mmHg
Molecular Formula C9H12N2O4 Melting Point 163-166ºC(lit.)
MSDS USA Flash Point 227.1±28.7 °C

 Names

Name [(1S,2S)-1,3-dihydroxy-1-(4-nitrophenyl)propan-2-yl]azanium
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Boiling Point 451.9±45.0 °C at 760 mmHg
Melting Point 163-166ºC(lit.)
Molecular Formula C9H12N2O4
Molecular Weight 212.203
Flash Point 227.1±28.7 °C
Exact Mass 212.079712
PSA 112.30000
LogP 0.13
Vapour Pressure 0.0±1.2 mmHg at 25°C
Index of Refraction 1.630
InChIKey OCYJXSUPZMNXEN-IUCAKERBSA-N
SMILES NC(CO)C(O)c1ccc([N+](=O)[O-])cc1

 Safety Information

Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3

 Articles5

More Articles
[Studies on the resolution of racemic gossypol. IV. Use of threo (-) or (+)-1-(p-nitrophenyl)-1,3-dihydroxypropylamine-2 as the resolving agent].

Yao Xue Xue Bao 25(6) , 430-4, (1990)

Threo (-) or (+)-1-(p-nitrophenyl)-1,3-dihydroxypropylamine-2 was found to be a useful resolving agent for racemic gossypol. The optical and chemical stability of the condensate of enantiomeric gossyp...

Investigation of Batten disease with the yeast Saccharomyces cerevisiae.

Mol. Genet. Metab. 66(4) , 314-9, (1999)

The CLN3 gene, which encodes the protein whose absence is responsible for Batten disease, the most common inherited neurovisceral storage disease of childhood, was identified in 1995. The function of ...

High-performance liquid chromatographic determination of chloramphenicol and 2-amino-1-(p-nitrophenyl)-1,3-propanediol in pharmaceutical formulations.

J. Chromatogr. A. 170(1) , 282-7, (1979)

 Bioassay

View more

Name: Antibacterial activity against methicillin-resistant Staphylococcus aureus N315 after...
Source: ChEMBL
Target: Staphylococcus aureus
External Id: CHEMBL3821869
Name: Antibacterial activity against Escherichia coli DH52 after 24 hrs by two fold serial ...
Source: ChEMBL
Target: Escherichia coli
External Id: CHEMBL3821873
Name: Antimicrobial activity against Bacillus subtilis ATCC 6633 after 24 hrs by microbroth...
Source: ChEMBL
Target: Bacillus spizizenii
External Id: CHEMBL3811120
Name: Antibacterial activity against Micrococcus luteus ATCC4698 after 24 hrs by two fold s...
Source: ChEMBL
Target: Micrococcus luteus
External Id: CHEMBL3821872
Name: Antimicrobial activity against Staphylococcus aureus ATCC 25923 after 24 hrs by micro...
Source: ChEMBL
Target: Staphylococcus aureus
External Id: CHEMBL3811119
Name: Antibacterial activity against Bacillus subtilis ATCC6633 after 24 hrs by two fold se...
Source: ChEMBL
Target: Bacillus subtilis
External Id: CHEMBL3821871
Name: Antimicrobial activity against methicillin-resistant Staphylococcus aureus N315 after...
Source: ChEMBL
Target: Staphylococcus aureus
External Id: CHEMBL3811118
Name: Antibacterial activity against Staphylococcus aureus ATCC25923 after 24 hrs by two fo...
Source: ChEMBL
Target: Staphylococcus aureus
External Id: CHEMBL3821870
Name: Antibacterial activity against Bacillus proteus ATCC13315 after 24 hrs by two fold se...
Source: ChEMBL
Target: Bacillus
External Id: CHEMBL3821877
Name: Antimicrobial activity against Bacillus proteus ATCC 13315 after 24 hrs by microbroth...
Source: ChEMBL
Target: Bacillus
External Id: CHEMBL3811124
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 Synonyms

2-Amino-1-(4-nitrophenyl)-1,3-propanediol
(-)-(1R,2R)-1-para-nitrophenyl-2-amino-1,3-propanediol
L-(+)-threo-2-Amino-1-(4-nitrophenyl)-1,3-propanediol
2-amino-1-(4-nitrophenyl)propane-1,3-diol
D-(-)-threo-2-Amino-1-(p-nitrophenyl)-1,3-propanediol
Threomine
(1R,2R)-(-)-2-amino-1-(4-nitrophenyl)-1,3-propanediol
D-threo-2-Amino-1-(4-nitrophenyl)-1,3-propanediol
D-threo-(-)-2-Amino-1-(p-nitrophenyl)-1,3-propanediol
MFCD00007359
1-(p-nitrophenyl)-2-amino-1,3-propanediol
(-)-(1R,2R)-1-(4'-nitrophenyl)-2-amino-1,3-propanediol
(1S,2S)-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol
(1S2S)-2-AMINO-1-(4-NITROPHENYL)PROPANE-13-DIOL
(1S,2S)
EINECS 221-001-4
(1S,2S)-2-Amino-1-(p-nitrophenyl)-1,3-propanediol
Adenosine DisopiuM Triphosphate
(2S)-2-aMino-1-(4-nitrophenyl)propane-1,3-diol
(2R,3R)-2-amino-3-hydroxy-3-(p-nitrophenyl)-1-propanol
(1S,2S)-2-Amino-1-(4-nitrophenyl)propane-1,3-diol
D-(+)-threo-1-P-nitrophenyl-2-amino-1,3-propanediol
[S(R*,R*)]-2-amino-1-(p-nitrophenyl)propane-1,3-diol
D-(-)-threo-2-amino-1-(4-nitrophenyl)-1,3-propanediol
L-BASE
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