193085-24-4

193085-24-4 - Names and Identifiers

Name	1-Boc-Piperidin-4-ylidene-acetic acid
Synonyms	1-Boc-4-Carboxymethylene-Piperidine 1-BOC-4-CARBOXYMETHYLENE-PIPERIDINE 1-Boc-Piperidin-4-Ylideneacetic Acid (1-Boc-4-piperidinylidene)acetic acid 1-Boc-piperidin-4-ylidene avetic acid 1-Boc-Piperidin-4-ylidene-acetic acid 1-Boc-Piperidin-4-Ylidene Avetic Acid 1-BOC-PIPERIDIN-4-YLIDENE-ACETIC ACID 1-N-Boc-Piperidin-4-Ylidene-Acetic Acid 1-N-Boc-Piperidin-4-ylidene-acetic acid 2-(1-Boc-piperidin-4-ylidene)acetic acid [1-(Tert-Butoxycarbonyl)Piperidin-4-Ylidene]Acetic Acid 2-(1-(Tert-Butoxycarbonyl)Piperidin-4-Ylidene)Acetic Acid 4-CARBOXYMETHYLENE-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 4-Carboxymethylene-Piperidine-1-Carboxylic Acid Tert-Butyl Ester 1-Boc-Piperidin-4-ylidene-acetic acid N-Boc-Piperidin-4-ylidene-acetic acid 2-(1-(tert-butoxycarbonyl)piperidin-4-ylidene)acetic acid
CAS	193085-24-4
InChI	InChI=1/C12H19NO4/c1-12(2,3)17-11(16)13-6-4-9(5-7-13)8-10(14)15/h8H,4-7H2,1-3H3,(H,14,15)

193085-24-4 - Physico-chemical Properties

Molecular Formula	C12H19NO4
Molar Mass	241.28
Density	1.228g/cm³
Boling Point	386.951°C at 760 mmHg
Flash Point	187.822°C
Vapor Presure	0mmHg at 25°C
Storage Condition	2-8°C
Refractive Index	1.564

193085-24-4 - Risk and Safety

Hazard Symbols	Xi - Irritant
Risk Codes	R36/37/38 - Irritating to eyes, respiratory system and skin. R36 - Irritating to the eyes
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
Hazard Class	IRRITANT

193085-24-4 - Introduction

The acid is an organic compound with the following properties:

1. Appearance: It is usually a white solid.

2. Solubility: It has good solubility in some common organic solvents (such as dimethylformamide, dichloromethane, etc.).

3. Stability: It is relatively stable under regular storage conditions and is not easy to decompose.

The acid is mainly used for the preparation of protecting groups in organic synthesis (a protecting group is a chemical group that protects a specific functional group from reaction in a chemical reaction) and intermediates. It can be used as synthetic acylating agents, ketonizing agents, and acyl nucleophiles, etc.

This compound can be obtained by the following preparation methods: first, piperidine-4-methylene acid is reacted with 1-boc-imine to obtain an intermediate of acid; Then, the target product is prepared by esterification with an appropriate acid.

Regarding safety information, acid is generally relatively safe under normal use and storage conditions. However, as a chemical, it is still dangerous. Appropriate laboratory techniques and personal protective measures, such as wearing gloves and protective glasses, should be taken during handling and use. At the same time, should be away from the fire and heat source to avoid its combustion. Detailed safety information can be obtained in the relevant chemical Safety Data Sheet (MSDS). It is recommended to learn more about the safe use guidelines of this compound before use.

Last Update：2024-04-09 21:11:58