1-Boc-piperidine-3-carboxylhydrazide

1-Boc-piperidine-3-carboxylhydrazide - Names and Identifiers

Name	1-Boc-Nipecotic acid hydrazide
Synonyms	1-BOC-NIPECOTIC ACID HYDRAZIDE 1-Boc-Nipecotic acid hydrazide 1-Boc-piperidine-3-carboxylhydrazide S-(N-Boc)-piperidine-3-carboxylhydrazide (S)-1-Boc-piperidine-3-carboxylic acid hydrazide tert-butyl 3-(hydrazinecarbonyl)piperidine-1-carboxylate (S)-tert-Butyl 1-(piperidine-3-carbonyl)hydrazinecarboxylate 3-HYDRAZINOLARBONYL-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 3-hydrazinolcarbonylpiperidine-1-carboxylic acid tert-butyl ester 3-HYDRAZINOCARBONYL-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
CAS	625470-88-4
InChI	InChI=1/C11H21N3O3/c1-11(2,3)17-10(16)14-6-4-5-8(7-14)9(15)13-12/h8H,4-7,12H2,1-3H3,(H,13,15)

1-Boc-piperidine-3-carboxylhydrazide - Physico-chemical Properties

Molecular Formula	C11H21N3O3
Molar Mass	243.3
Density	1.147g/cm³
Boling Point	409.2°C at 760 mmHg
Flash Point	201.3°C
Vapor Presure	6.6E-07mmHg at 25°C
Storage Condition	Room Temprature
Refractive Index	1.507

1-Boc-piperidine-3-carboxylhydrazide - Risk and Safety

Hazard Symbols	Xn - Harmful
Risk Codes	22 - Harmful if swallowed
Hazard Class	IRRITANT

1-Boc-piperidine-3-carboxylhydrazide - Introduction

1-Boc-Nipoctic acid hydrazide, also known as 1-Boc-Nipoctic acid hydrazide, is an organic compound. The following is an introduction to its nature, use, preparation and safety information:

Nature:
1-Boc-Nipoctic acid hydrazide is a solid with a white crystalline appearance. It is stable at room temperature, but decomposes at high temperatures. It is less soluble in water and soluble in organic solvents such as ethanol and dimethyl sulfoxide.

Use:
1-Boc-Nipoctic acid hydrazide is an important intermediate in organic synthesis. It can be used to synthesize bioactive molecules such as drugs and pesticides. It is commonly used in the pharmaceutical field for the synthesis of compounds with central nervous system activity, such as antipsychotic drugs.

Preparation Method:
1-Boc-Nipoctic acid hydrazide are generally prepared by chemical reaction. A common method is to react 3-piperidinecarboxylic acid with formic acid hydrazine, and then introduce a BOC protecting group (t-butoxycarbyl) into the molecule through esterification. The reaction is generally carried out in a suitable solvent under an inert atmosphere.

Safety Information:
1-Boc-Nipoctic acid hydrazide requires safety during use and storage. It may be irritating to the eyes, skin and respiratory system, so wear protective equipment such as gloves, goggles and protective masks during operation. In addition, it may also have an adverse impact on the environment, and care should be taken to prevent its leakage and discharge into the environment.

Last Update：2024-04-09 20:52:54