3-(2-Carboxy-acetyl)-piperidine-1-carboxylic acid benzyl ester
3-(1-benzyloxycarbonyl-3-piperidyl)-3-oxo-propanoic acid
CAS: 886362-40-9
Molecular Formula: C16H19NO5
3-(2-Carboxy-acetyl)-piperidine-1-carboxylic acid benzyl ester - Names and Identifiers
| Name | 3-(1-benzyloxycarbonyl-3-piperidyl)-3-oxo-propanoic acid |
| Synonyms | 3-(1-benzyloxycarbonyl-3-piperidyl)-3-oxo-propanoic acid 3-(1-(benzyloxycarbonyl)piperidin-3-yl)-3-oxopropanoic acid 3-(2-Carboxy-acetyl)-piperidine-1-carboxylic acid benzyl ester beta-Oxo-1-[(phenylmethoxy)carbonyl]-3-piperidinepropanoic acid 3-Piperidinepropanoic acid, .beta.-oxo-1-[(phenylmethoxy)carbonyl]- |
| CAS | 886362-40-9 |
| InChI | InChI=1/C16H19NO5/c18-14(9-15(19)20)13-7-4-8-17(10-13)16(21)22-11-12-5-2-1-3-6-12/h1-3,5-6,13H,4,7-11H2,(H,19,20) |
3-(2-Carboxy-acetyl)-piperidine-1-carboxylic acid benzyl ester - Physico-chemical Properties
| Molecular Formula | C16H19NO5 |
| Molar Mass | 305.326 |
| Density | 1.281 |
| Boling Point | 502.5°C at 760 mmHg |
| Flash Point | 257.7°C |
| Vapor Presure | 6.44E-11mmHg at 25°C |
| Refractive Index | 1.563 |
3-(2-Carboxy-acetyl)-piperidine-1-carboxylic acid benzyl ester - Introduction
3-(benzyloxy)-3-oxo-propanoic acid, also known as 3-(1-benzyloxycarbonyl-3-piperidinyl)-3-oxopropionic acid, is an organic compound.
Nature:
3-oxo-propanic acid is a white or yellowish solid with a special odor. Its chemical formula is C19H21NO5 and its relative molecular mass is 351.377. The compound has inhibitory activity and is a multifunctional agent.
Use:
3-oxo-propanic acid is widely used in chemical synthesis. It is often used as an intermediate in the synthesis of pharmaceuticals for the synthesis of biologically active compounds. It can also be used for protecting group conversion reactions in organic synthesis.
Preparation Method:
The preparation of (br)-3-oxo-propanic acid usually uses piperidine as a starting material. A common preparation method is to first protect the amino group of piperidine as a N-Cbz group using chloroformyl chloride and then introduce an acetyl group onto piperidine via an acylation reaction.
Safety Information:
Regarding the safety of 3-(3-oxo-propanoic acid), general laboratory safety procedures need to be followed in chemical operations. In handling the compound, care should be taken to prevent skin contact, inhalation or ingestion. During use, wear appropriate personal protective equipment, such as laboratory coats, gloves and glasses. After treatment, the waste of the compound should be properly disposed.
Nature:
3-oxo-propanic acid is a white or yellowish solid with a special odor. Its chemical formula is C19H21NO5 and its relative molecular mass is 351.377. The compound has inhibitory activity and is a multifunctional agent.
Use:
3-oxo-propanic acid is widely used in chemical synthesis. It is often used as an intermediate in the synthesis of pharmaceuticals for the synthesis of biologically active compounds. It can also be used for protecting group conversion reactions in organic synthesis.
Preparation Method:
The preparation of (br)-3-oxo-propanic acid usually uses piperidine as a starting material. A common preparation method is to first protect the amino group of piperidine as a N-Cbz group using chloroformyl chloride and then introduce an acetyl group onto piperidine via an acylation reaction.
Safety Information:
Regarding the safety of 3-(3-oxo-propanoic acid), general laboratory safety procedures need to be followed in chemical operations. In handling the compound, care should be taken to prevent skin contact, inhalation or ingestion. During use, wear appropriate personal protective equipment, such as laboratory coats, gloves and glasses. After treatment, the waste of the compound should be properly disposed.
Last Update：2024-04-09 21:54:55
Supplier List
View History
3-(2-Carboxy-acetyl)-piperidine-1-carboxylic acid benzyl ester
hexandraside D
Methyl 7-bromo-2,3-dihydrobenzofuran-3-carboxylate
42899-59-2
N-Butyl-3-Methylpyridinium Chloride
7-Methyl-1H-indazole-5-boronic acid pinacol ester
4-(3,4-dimethylphenyl)-2-[3-(4-fluorophenyl)-5-(4-isopropylphenyl)-4,5-dihydro-1H-pyrazol-1-yl]-1,3-thiazole
1-((2R,3S,4R,5R)-3,4-dihydroxy-5-(hydroxyMethyl)-3-Methyltetrahydrofuran-2-yl)pyriMidine-2,4(1H,3H)-dione
9,10-Anthracenedione, 4,8-diamino-2-(4-(2-ethoxyethoxy)phenyl)-1,5-dihydroxy-
N,N,N',N'-Tetramethyl-2,2-dimethyl-1,3-propanediamine
hexandraside D
Methyl 7-bromo-2,3-dihydrobenzofuran-3-carboxylate
42899-59-2
N-Butyl-3-Methylpyridinium Chloride
7-Methyl-1H-indazole-5-boronic acid pinacol ester
4-(3,4-dimethylphenyl)-2-[3-(4-fluorophenyl)-5-(4-isopropylphenyl)-4,5-dihydro-1H-pyrazol-1-yl]-1,3-thiazole
1-((2R,3S,4R,5R)-3,4-dihydroxy-5-(hydroxyMethyl)-3-Methyltetrahydrofuran-2-yl)pyriMidine-2,4(1H,3H)-dione
9,10-Anthracenedione, 4,8-diamino-2-(4-(2-ethoxyethoxy)phenyl)-1,5-dihydroxy-
N,N,N',N'-Tetramethyl-2,2-dimethyl-1,3-propanediamine