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Merck
CN

471674

(1S,2S)-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol

99%

Synonym(s):

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

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About This Item

Linear Formula:
O2NC6H4CH(OH)CH(NH2)CH2OH
CAS Number:
2964-48-9
Molecular Weight:
212.20
NACRES:
NA.22
PubChem Substance ID:
24870752
UNSPSC Code:
12352116
EC Number:
221-001-4
MDL number:
MFCD00007359
Assay:
99%

Key Documents

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Product Name

(1S,2S)-(+)-2-Amino-1-(4-nitrophenyl)-1,3-propanediol, 99%

InChI key

OCYJXSUPZMNXEN-IUCAKERBSA-N

InChI

1S/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/t8-,9-/m0/s1

SMILES string

N[C@@H](CO)[C@@H](O)c1ccc(cc1)[N+]([O-])=O

assay

99%

optical activity

[α]23/D +31°, c = 1 in 6 M HCl

mp

163-166 °C (lit.)

functional group

amine
hydroxyl
nitro

Quality Level

100

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ4489
MKCM3136
MKCF1522
MKBT1020V
MKBR0379V

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D A Pearce et al.
Molecular genetics and metabolism, 66(4), 314-319 (1999-04-07)
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 the protein, Cln3p, still remains elusive. We previously cloned the
D K Zheng et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 25(6), 430-434 (1990-01-01)
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 gossypols with the titled amine and the great difference in the Rf values on TLC
Induced synthesis of phosphatases in Anacystis nidulans by p-NO2-phenylserinal.
M L Muñoz-Calvo et al.
The Journal of antibiotics, 33(5), 520-522 (1980-05-01)
W A Korfmacher et al.
Journal of chromatographic science, 28(5), 236-238 (1990-05-01)
The thermospray (TS) liquid chromatographic-mass spectrometric analysis of the antibiotic chloramphenicol and three related compounds is presented. The three additional compounds are dehydrochloramphenicol, aminodehydrochloramphenicol, and nitrophenylaminopropanediol. Baseline separation of the four compounds is achieved. The TS mass spectrum of each
High-performance liquid chromatographic determination of chloramphenicol and 2-amino-1-(p-nitrophenyl)-1,3-propanediol in pharmaceutical formulations.
M J LeBelle et al.
Journal of chromatography, 170(1), 282-287 (1979-02-11)

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