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L-Phenylalaninol, 98%, Thermo Scientific Chemicals
27.80 € - 344.00 €
Chemical Identifiers
| CAS | 3182-95-4 |
|---|---|
| Molecular Formula | C9H13NO |
| Molecular Weight (g/mol) | 151.21 |
| MDL Number | MFCD00004732 |
| InChI Key | STVVMTBJNDTZBF-VIFPVBQESA-N |
| Synonym | l-phenylalaninol, s-2-amino-3-phenyl-1-propanol, s---2-amino-3-phenyl-1-propanol, s-2-amino-3-phenylpropan-1-ol, h-phenylalaninol, h-phe-ol, 2s-2-amino-3-phenylpropan-1-ol, phenylalaninol, --l-phenylalaninol, l-phenyl alaninol |
| PubChem CID | 447213 |
| IUPAC Name | (2S)-2-amino-3-phenylpropan-1-ol |
| SMILES | N[C@H](CO)CC1=CC=CC=C1 |
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|---|---|---|---|---|---|---|---|---|---|
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|
11484653
|
Thermo Scientific Alfa Aesar
A11586.03 |
1 g |
27.80 €
1g |
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|
11494653
|
Thermo Scientific Alfa Aesar
A11586.06 |
5 g |
88.60 €
5g |
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|
11404663
|
Thermo Scientific Alfa Aesar
A11586.14 |
25 g |
344.00 €
25g |
Please sign in to purchase this item. Need a web account? Register with us today! | |||||
Description
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.
ApplicationsL-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.
Chemical Identifiers
| 3182-95-4 | |
| 151.21 | |
| STVVMTBJNDTZBF-VIFPVBQESA-N | |
| 447213 | |
| N[C@H](CO)CC1=CC=CC=C1 |
| C9H13NO | |
| MFCD00004732 | |
| l-phenylalaninol, s-2-amino-3-phenyl-1-propanol, s---2-amino-3-phenyl-1-propanol, s-2-amino-3-phenylpropan-1-ol, h-phenylalaninol, h-phe-ol, 2s-2-amino-3-phenylpropan-1-ol, phenylalaninol, --l-phenylalaninol, l-phenyl alaninol | |
| (2S)-2-amino-3-phenylpropan-1-ol |
Specifications
| 3182-95-4 | |
| −23° (c=5 in ethanol) | |
| MFCD00004732 | |
| 2208238 | |
| STVVMTBJNDTZBF-VIFPVBQESA-N | |
| (2S)-2-amino-3-phenylpropan-1-ol | |
| 447213 | |
| 98% |
| 89°C to 94°C | |
| C9H13NO | |
| UN3259 | |
| l-phenylalaninol, s-2-amino-3-phenyl-1-propanol, s---2-amino-3-phenyl-1-propanol, s-2-amino-3-phenylpropan-1-ol, h-phenylalaninol, h-phe-ol, 2s-2-amino-3-phenylpropan-1-ol, phenylalaninol, --l-phenylalaninol, l-phenyl alaninol | |
| N[C@H](CO)CC1=CC=CC=C1 | |
| 151.21 | |
| 151.21 | |
| L-Phenylalaninol |
Safety and Handling
GHS H Statement
H314-H318
Causes severe skin burns and eye damage.
Causes serious eye damage.
GHS P Statement
P280-P303+P361+P353-P305+P351+P338-P310
Wear protective gloves/protective clothing/eye protection/face protection.
IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower.
IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do.
Continue rinsing.
Immediately call a POISON CENTER or doctor/physician.
Danger
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missing translation for 'rtecsNumber' : UA6900000
RUO – Research Use Only
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