167262-68-2

167262-68-2 - Names and Identifiers

Name	BOC-4-phenylpiperidine-4-Carboxylic acid
Synonyms	RARECHEM EM WB 0182 BOC-4-phenylpiperidine-4-Carboxylic acid BOC-4-PHENYLPIPERIDINE-4-CARBOXYLIC ACID N-BOC-4-PHENYL-4-piperidinecarboxylic acid 1-BOC-4-phenylpiperidine-4-carboxylic acid 1-(tert-butoxycarbonyl)-4-phenylpiperidine-4-carboxylate 1-(tert-butoxycarbonyl)-4-phenylpiperidine-4-carboxylic acid 1-(TERT-BUTOXYCARBONYL)-4-PHENYL-4-PIPERIDINECARBOXYLIC ACID 1-(tert-butoxycarbonyl)-4-PHENYL-4-piperidinecarboxylic acid 4-PHENYL-PIPERIDINE-1,4-Dicarboxylic acid MONO-TERT-BUTYL ESTER 4-PHENYL-PIPERIDINE-1,4-DICARBOXYLIC ACID MONO-TERT-BUTYL ESTER 1-[[(tert-Butyl)oxy]carbonyl]-4-phenyl-4-piperidinecarboxylic acid 1,4-Piperidinedicarboxylicacid, 4-phenyl-, 1-(1,1-dimethylethyl) ester
CAS	167262-68-2
InChI	InChI=1/C17H23NO4/c1-16(2,3)22-15(21)18-11-9-17(10-12-18,14(19)20)13-7-5-4-6-8-13/h4-8H,9-12H2,1-3H3,(H,19,20)/p-1

167262-68-2 - Physico-chemical Properties

Molecular Formula	C17H23NO4
Molar Mass	305.37
Density	1.176
Melting Point	187-189°C
Boling Point	450°C at 760 mmHg
Flash Point	226°C
Vapor Presure	6.93E-09mmHg at 25°C
Storage Condition	Store at 0-5°C
Physical and Chemical Properties	Storage Conditions: Store at 0-5 ℃

167262-68-2 - Risk and Safety

HS Code	29333990
Hazard Class	IRRITANT

167262-68-2 - Introduction

BOC-4-phenylpiperidine-4-Carboxylic acid is an organic compound whose structure contains a Boc protecting group (tert-butyloxycarbonyl) at the 4-position of the piperidinecarboxylic acid and a phenyl group (phenyl ring) at the 1-position of the piperidinecarboxylic acid.

Nature:
BOC-4-phenylpiperidine-4-Carboxylic acid is a white crystalline solid with low solubility. Its molecular formula is C16H19NO4 and its relative molecular mass is 297.33g/mol.

Use:
BOC-4-phenylpiperidine-4-Carboxylic acid is an important intermediate in organic synthesis. It is commonly used in the preparation of piperidinecarboxylic acids and other organic compounds, and has a wide range of applications in the synthesis of drugs, pesticides, pigments, coatings and polymers.

Method:
BOC-4-phenylpiperidine-4-Carboxylic acids are usually prepared by chemical synthesis from the corresponding starting materials. Specific preparation methods often involve the reaction of piperidine with benzyl alcohol, followed by the introduction of a protecting group (Boc) into the reaction product. This step is typically accomplished by reaction with Mono (t-Bu) carbonate under acidic conditions.

Safety Information:
BOC-4-phenylpiperidine-4-Carboxylic acid is relatively stable at room temperature, it should be kept away from heat sources and flames, and avoid contact with strong oxidants. It may cause irritation to the eyes, skin and respiratory tract, so wear appropriate protective equipment when using it. Appropriate laboratory safety practices should be followed during storage and handling.

Last Update：2024-04-09 20:49:11