CAS 2964-48-9
:(1S,2S)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol
Description:
(1S,2S)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol, with the CAS number 2964-48-9, is an organic compound characterized by its amino alcohol structure. It features a chiral center, which contributes to its stereochemistry, specifically the (1S,2S) configuration. The presence of a 4-nitrophenyl group indicates that it has a nitro substituent on a phenyl ring, which can influence its reactivity and polarity. This compound is typically a solid at room temperature and is soluble in polar solvents due to the hydroxyl and amino functional groups. Its amino group can participate in hydrogen bonding, enhancing its solubility in aqueous environments. The nitro group may also impart specific electronic properties, making it useful in various chemical applications, including as an intermediate in organic synthesis or in pharmaceuticals. Overall, the unique combination of functional groups and stereochemistry makes this compound of interest in both research and industrial contexts.
Formula:C9H12N2O4
InChI:InChI=1/C9H12N2O4/c10-8(5-12)9(13)6-1-3-7(4-2-6)11(14)15/h1-4,8-9,12-13H,5,10H2/p+1/t8-,9-/m0/s1
InChI key:InChIKey=OCYJXSUPZMNXEN-IUCAKERBSA-N
SMILES:[C@H]([C@H](CO)N)(O)C1=CC=C(N(=O)=O)C=C1
Synonyms:- (1R,2R)-2-amino-1-(4-nitrophenyl)propane-1,3-diol
- (1S,2S)-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol
- (1S,2S)-1,3-dihydroxy-1-(4-nitrophenyl)propan-2-aminium
- (2S,3S)-2-Amino-3-(4-nitrophenyl)propane-1,3-diol
- 1,3-Propanediol, 2-amino-1-(4-nitrophenyl)-, (1S,2S)-
- 1,3-Propanediol, 2-amino-1-(4-nitrophenyl)-, [S-(R*,R*)]-
- 1,3-Propanediol, 2-amino-1-(p-nitrophenyl)-, <span class="text-smallcaps">L</span>-threo-(+)-
- <span class="text-smallcaps">L</span>-(+)-threo-1-(p-Nitrophenyl)-2-amino-1,3-propanediol
- <span class="text-smallcaps">L</span>-(p-Nitrophenyl)-2-amino-1,3-propanediol
- <span class="text-smallcaps">L</span>-1-(p-Nitrophenyl)-2-aminopropane-1,3-diol
- <span class="text-smallcaps">L</span>-threo-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol
- Dextramine
- L-(+)-threo
- L-(+)-threo-2-Amino-1-(4-nitrophenyl)-1,3-propanediol
- NSC 12466
- Threomine
- threo-(1S,2S)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol
- 1,3-Propanediol, 2-amino-1-(p-nitrophenyl)-, L-threo-(+)-
- (1S,2S)-
- (1S,2S)-2-Amino-1-(p-nitrophenyl)-1,3-propanediol
- (1S,2S)-2-AMino-1-(4-nitrophenyl)propane-1,3-diol, 96% 5GR
- (1S2S)-2-AMINO-1-(4-NITROPHENYL)PROPANE-13-DIOL 96%
- (1S,2S)-2-Amino-1-(4-nitrophenyl)propane-1,3-diol,96%
- L-BASE
- D-amino-compound
- [S(R*,R*)]-2-amino-1-(p-nitrophenyl)propane-1,3-diol
- (2S)-2-aMino-1-(4-nitrophenyl)propane-1,3-diol
- Adenosine DisopiuM Triphosphate
- (1S,2S)-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol 99%
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 8 products.
(1S,2S)-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol
CAS:Formula:C9H12N2O4Purity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:212.212-amino-1-(4-nitrophenyl)propane-1,3-diol
CAS:2-amino-1-(4-nitrophenyl)propane-1,3-diolColor and Shape:White Powder1,3-Propanediol, 2-amino-1-(4-nitrophenyl)-, (1S,2S)-
CAS:Formula:C9H12N2O4Purity:98%Color and Shape:SolidMolecular weight:212.2026(1S,2S)-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol
CAS:<p>(1S,2S)-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol</p>Purity:98%Color and Shape:SolidMolecular weight:212.20g/molL-threo-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol
CAS:Controlled Product<p>Applications Used in the synthesis of (4S,5S)-(-)-isocytoxazone.<br>References Kakeya, H., et al.: J. Antibiot., 51, 1126 (1998), Carter, P., et al.: Bioorg. Med. Chem. Lett., 13, 1237 (2003),<br></p>Formula:C9H12N2O4Color and Shape:Off-WhiteMolecular weight:212.20(1S,2S)-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol
CAS:Formula:C9H12N2O4Purity:95%Color and Shape:Solid, Off-white powderMolecular weight:212.205L-threo-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol
CAS:<p>L-threo-(+)-2-amino-1-(4-nitrophenyl)-1,3-propanediol is a functional group that is composed of a fatty acid and an amino acid. It has been shown to inhibit the growth of corynebacterium glutamicum bacteria by hydrolyzing their cell wall. This compound also inhibits the activity of bacterial enzymes that are involved in the synthesis of proteins. This functional group may be useful for the treatment of chronic lymphocytic leukemia and HIV infection.</p>Formula:C9H12N2O4Purity:Min. 95%Color and Shape:PowderMolecular weight:212.2 g/mol








