Carbamic acid, N-[(1R)-3-chloro-2-oxo-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester - Names and Identifiers
Name | (3R)-3-(N-Boc-amino)-1-chloro-4-phenyl-2-butanone
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Synonyms | Boc-D-Phe chloromethyl ketone (3R)-3-(N-Boc-amino)-1-chloro-4-phenyl-2-butanone (R)-tert-Butyl (4-chloro-3-oxo-1-phenylbutan-2-yl)carbamate Carbamic acid, N-[(1R)-3-chloro-2-oxo-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester
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CAS | 150935-37-8
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InChI | InChI=1/C15H20ClNO3/c1-15(2,3)20-14(19)17-12(13(18)10-16)9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,19)/t12-/m1/s1 |
Carbamic acid, N-[(1R)-3-chloro-2-oxo-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester - Physico-chemical Properties
Molecular Formula | C15H20ClNO3
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Molar Mass | 297.78 |
Storage Condition | 2-8°C |
Refractive Index | 1.517 |
Carbamic acid, N-[(1R)-3-chloro-2-oxo-1-(phenylmethyl)propyl]-, 1,1-dimethylethyl ester - Introduction
(3R)-3-(N-Boc-amino)-is an organic compound with the following properties:
1. Appearance: common for white solid.
2. Molecular formula: C13H17ClNO3.
3. Relative molecular mass: 277.73.
4. Melting point: About 118-122 ° C.
5. Solubility: Soluble in common organic solvents, such as dimethyl sulfoxide and dichloromethane.
6. Preservation: need to be stored in low temperature, dry, dark and well ventilated place.
(3R)-3-(N-Boc-amino):
1. Organic Synthesis: as acylation reagent, can be used for the synthesis of peptide compounds.
2. Drug research: for the synthesis of drugs and bioactive molecules.
3. Neuroscience research: as a raw material for the synthesis of neurotransmitter derivatives.
(3R)-3-(N-Boc-amino)-Preparation method:
The compound can be prepared by the following steps:
1. Acylation of D-phenylalanine with Boc-iminoic acid to give Boc-D-phenylalanine.
2. React phenylalanine with chloroformic acid to generate (3R)-3-(N-Boc-amino)-Boc-D acylation.
Safety Information:
1. Wear appropriate protective equipment during operation, including acid and alkali resistant gloves, goggles and laboratory coats.
2. Avoid contact with skin and inhalation of dust to avoid allergy or irritation.
3. Keep the laboratory well ventilated to avoid the accumulation of toxic substances.
4. During storage and handling, avoid contact with oxidants to avoid fire or explosion.
Please note that when conducting any chemical experiments, make sure to follow the correct safety procedures, and refer to relevant literature and safety data forms for more detailed information.
Last Update:2024-04-09 15:17:52