[A11586] CAS 3182-95-4 | L-Phenylalaninol, 98% | Alfa
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Brand: Alfa Aesar
3182-95-4 | C9H13NO | (S)-β-aminobenzenepropanol
Chemical Identifiers
CAS
3182-95-4
Molecular Weight (g/mol)
151.21
MDL Number
MFCD00004732
Synonym
L-phenylalaninol|2-amino-3-phenyl-1-propanol|S-phenylalaninol|(S)-2-benzylethanolamine|(R)-2-amino-3-phenylpropanol|(S)-β-aminobenzenepropanol
SMILES
N[C@H](CO)CC1=CC=CC=C1
InChI Key
STVVMTBJNDTZBF-VIFPVBQESA-N
Molecular Formula
C9H13NO
IUPAC Name
(2S)-2-amino-3-phenylpropan-1-ol
Specifications
Melting Point (clear melt)
88.0-94.0°C
Optical Rotation
-23.3 to -25.3° (C=5 in ethanol)
Appearance (Color)
White to cream to yellow
Form
Crystals or powder or crystalline powder
Assay (Non-aqueous acid-base Titration)
≥97.5 to ≤102.5%
설명
L-Phenylalaninol acts as an antiulcer agent that reduces the secretion of gastric acid and prevents ulcer formation. It inhibits intestinal absorption of L-phenylalanine making it a prospective treatment for phenylketonuria. Further, it reacts with nitriles to form oxazolines, which finds application in palladium-catalyzed allylic substitution. In addition to this, it is also used in amidation for chiral resolution and nicotinamide adenine dinucleotide modeling.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
L-Phenylalaninol acts as an antiulcer agent that reduces the secretion of gastric acid and prevents ulcer formation. It inhibits intestinal absorption of L-phenylalanine making it a prospective treatment for phenylketonuria. Further, it reacts with nitriles to form oxazolines, which finds application in palladium-catalyzed allylic substitution. In addition to this, it is also used in amidation for chiral resolution and nicotinamide adenine dinucleotide modeling.
L-Phenylalaninol acts as an antiulcer agent that reduces the secretion of gastric acid and prevents ulcer formation. It inhibits intestinal absorption of L-phenylalanine making it a prospective treatment for phenylketonuria. Further, it reacts with nitriles to form oxazolines, which finds application in palladium-catalyzed allylic substitution. In addition to this, it is also used in amidation for chiral resolution and nicotinamide adenine dinucleotide modeling.
Solubility
Soluble in chloroform, ethyl acetate, ethanol and methanol.
Notes
Incompatible with acids, acid chlorides, acid anhydrides and oxidizing agents.
Other References:
UN Number:UN3259Beilstein:2208238
GHS Hazard and Precautionary Statements
Hazard Statements:H314
GHS H StatementH314-H318 Causes severe skin burns and eye damage. Causes serious eye damage.
Precautionary Statements:P260-P264b-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P501c
Risk & Safety
TSCA:NoRTECS Number:UA6900000
경고:RUO – Research Use Only
CAS3182-95-4FORMULAC9H13NOHAZARD CLASS8EINECS221-674-4MDLMFCD00004732PACKAGING GROUPIII
| Pakage | 1g, 25g, 5g |
|---|---|
| brand | Alfa Aesar |
