D-4-AMINOPHENYLALANINE
- CAS NO.:102281-45-8
- Empirical Formula: C9H12N2O2
- Molecular Weight: 180.2
- MDL number: MFCD00069926
- SAFETY DATA SHEET (SDS)
- Update Date: 2023-05-15 10:43:51
What is D-4-AMINOPHENYLALANINE?
The Uses of D-4-AMINOPHENYLALANINE
(2R)-2-Amino-3-(4-aminophenyl)propanoic Acid is an amino acid that is used as a reactant in the development of human calcitonin gene-related peptide (CGRP) receptor antagonists for treatment of acute migraine.
Definition
ChEBI: 4-amino-D-phenylalanine is the D-enantiomer of 4-aminophenylalanine. It is an enantiomer of a 4-amino-L-phenylalanine.
Properties of D-4-AMINOPHENYLALANINE
Melting point: | 268-270 °C(lit.) |
Boiling point: | 383.5±32.0 °C(Predicted) |
Density | 1.289±0.06 g/cm3(Predicted) |
storage temp. | Keep in dark place,Inert atmosphere,Room temperature |
solubility | H2O: 20 mg/mL, soluble |
form | white powder |
pka | 2.14±0.10(Predicted) |
CAS DataBase Reference | 102281-45-8(CAS DataBase Reference) |
Safety information for D-4-AMINOPHENYLALANINE
Computed Descriptors for D-4-AMINOPHENYLALANINE
New Products
4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Diclofenac Sodium IP/BP/EP/USP Mefenamic Acid IP/BP/EP/USP Ornidazole IP Diclofenac Potassium SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
BOC-PHE(3,5-DII,4-NH2)-OH
Fmoc-4-nitro-L-phenylalanine
FMOC-L-4-AMINOPHENYLALANINE(BOC)
(S)-4-NITROPHENYLALANINE METHYL ESTER HYDROCHLORIDE
H-P-AMINO-D-PHE-OH HCL
FMOC-D-4-AMINOPHENYLALANINE
Boc-p(NH-Z)-L-Phe-OH
N-ME-P-NITRO-PHE-OH
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