1-Boc-4-(4-chlorophenyl)-4-carboxypiperidine - Names and Identifiers
Name | 1,4-Piperidinedicarboxylic acid, 4-(4-chlorophenyl)-,1-(1,1-dimethylethyl) ester
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Synonyms | 1-Boc-4-(4-chlorophenyl)-4-carboxypiperidine BOC-4-(4-CHLOROPHENYL)-PIPERIDINE-4-CARBOXYLIC ACID 1-Boc-4-(4-chlorophenyl)-4-piperidinecarboxylic acid N-BOC-4-(P-CHLOROPHENYL)-4-PIPERIDINE CARBOXYLIC ACID 1-BOC-4-(4-CHLOROPHENYL)-4-PIPERIDINEDICARBOXYLIC ACID 1,4-Piperidinedicarboxylic acid, 4-(4-chlorophenyl)-,1-(1,1-... 1-(TERT-BUTOXYCARBONYL)-4-(4-CHLOROPHENYL)PIPERIDINE-4-CARBOXYLIC ACID 1,4-Piperidinedicarboxylic acid, 4-(4-chlorophenyl)-,1-(1,1-dimethylethyl) ester
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CAS | 644981-94-2
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1-Boc-4-(4-chlorophenyl)-4-carboxypiperidine - Physico-chemical Properties
Molecular Formula | C17H22ClNO4
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Molar Mass | 339.81 |
Storage Condition | Room Temprature |
1-Boc-4-(4-chlorophenyl)-4-carboxypiperidine - Risk and Safety
1-Boc-4-(4-chlorophenyl)-4-carboxypiperidine - Introduction
1,4-Piperidinedicarboxylic acid, 4-(4-chlorophenyl)-,1-(1,1-dimethylethyl) ester(1,4-Piperidinedicarboxylic acid, 4-(4-chlorophenyl)-,1-(1,1-dimethylethyl) ester is also known as a BOC-DPC BOC-DPC-Cl.
Nature:
1,4-Piperidinedicarboxylic acid, 4-(4-chlorophenyl)-,1-(1,1-dimethylethyl) ester is a white or off-white crystalline powder. Its molecular formula is C18H23ClNO4 and its relative molecular mass is 353.83g/mol. It is a stable solid, not easily soluble in water, but soluble in organic solvents such as dimethylformamide and chloroform.
Use:
1,4-Piperidinedicarboxylic acid, 4-(4-chlorophenyl)-,1-(1,1-dimethylethyl) ester are mainly used as intermediates in organic synthesis. It can be used to synthesize new drug molecules, drug precursors, pesticides and heterocyclic compounds. The BOC protecting group of the compound can protect other functional groups during the synthesis.
Preparation Method:
1,4-Piperidinedicarboxylic acid, 4-(4-chlorophenyl)-,1-(1,1-dimethylethyl) ester can be prepared by reacting 4-piperidinemethosulfate with a 1,4-dichlorobutane derivative. The preparation involves the synthesis of the piperidine ring and the substituted phenyl group, followed by esterification of the acid.
Safety Information:
1,4-Piperidinedicarboxylic acid, 4-(4-chlorophyll)-,1-(1,1-dimenthylethyl) ester is less toxic, but it is still necessary to maintain appropriate laboratory safety operations. Wear appropriate protective equipment during operation to avoid inhalation, skin contact and eating. In case of accidental contact or inhalation, the affected area should be cleaned promptly and medical advice should be sought if necessary.
Last Update:2024-04-09 02:00:47