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About This Item
Linear Formula:
4-(HO)C6H3(Cl)CH2CH(NH2)CO2H
CAS Number:
Molecular Weight:
215.63
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
NACRES:
NA.22
EC Number:
231-050-3
MDL number:
Quality Level
assay
97%
optical activity
[α]24/D −2°, c = 1 in 1 M HCl
reaction suitability
reaction type: solution phase peptide synthesis
mp
249 °C (lit.)
application(s)
peptide synthesis
SMILES string
N[C@@H](Cc1ccc(O)c(Cl)c1)C(O)=O
InChI
1S/C9H10ClNO3/c10-6-3-5(1-2-8(6)12)4-7(11)9(13)14/h1-3,7,12H,4,11H2,(H,13,14)/t7-/m0/s1
InChI key
ACWBBAGYTKWBCD-ZETCQYMHSA-N
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Michael Holzer et al.
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Carbamylation of proteins through reactive cyanate has been demonstrated to predict an increased cardiovascular risk. Cyanate is formed in vivo by breakdown of urea and at sites of inflammation by the phagocyte protein myeloperoxidase. Because myeloperoxidase (MPO) associates with high-density
Matthew P Curtis et al.
Chemical research in toxicology, 24(3), 418-428 (2011-02-16)
The persistent activation of innate immune cells in chronic inflammation is gaining recognition as a contributing factor in a number of human diseases. A distinguishing feature of activated leukocytes at sites of inflammation is their production of reactive species such
Mariusz G Fleszar et al.
Molecules (Basel, Switzerland), 25(21) (2020-11-11)
Quantification with satisfactory specificity and sensitivity of free 3-Nitro-l-tyrosine (3-NT), 3-Chloro-l-tyrosine (3-CT), and 3-Bromo-l-tyrosine (3-BT) in biological samples as potential inflammation, oxidative stress, and cancer biomarkers is analytically challenging. We aimed at developing a liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based method
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 512443-1G | 04061826102268 |