1-Boc-piperazine-2-Carbocylic acid

1-Boc-piperazine-2-Carbocylic acid - Names and Identifiers

Name	4-Boc-Piperazine-3-carboxylic acid
Synonyms	1-Boc-2-Piperazinecarboxylic acid 4-Boc-Piperazine-3-carboxylic acid 1-Boc-piperazine-2-Carbocylic acid 1-Boc-piperazine-2-carboxylic acid 4-Boc-Piperazine-3-carboxylic acidd 1,2-Piperazinedicarboxylic acid, 1-(1,1-diMethylethyl) ester 1-[(2-methylpropan-2-yl)oxycarbonyl]piperazine-2-carboxylic acid 1-{[(2-Methyl-2-propanyl)oxy]carbonyl}-2-piperazinecarboxylic acid
CAS	1214196-85-6
InChI	InChI=1S/C10H18N2O4/c1-10(2,3)16-9(15)12-5-4-11-6-7(12)8(13)14/h7,11H,4-6H2,1-3H3,(H,13,14)

1-Boc-piperazine-2-Carbocylic acid - Physico-chemical Properties

Molecular Formula	C10H18N2O4
Molar Mass	230.26
Density	1.193±0.06 g/cm3(Predicted)
Boling Point	371.8±37.0 °C(Predicted)
pKa	2.90±0.20(Predicted)
Storage Condition	under inert gas (nitrogen or Argon) at 2–8 °C

1-Boc-piperazine-2-Carbocylic acid - Risk and Safety

Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

1-Boc-piperazine-2-Carbocylic acid - Introduction

4-N-Boc-3-piperazinecarboxylic acid is an organic compound with the chemical name N-(tert-Butoxycarbonyl)-3-piperidinemethanoic acid(N-(Boc)-3-piperidinemethanoic acid). The following is a description of the properties, uses, preparation and safety information of the compound:

Nature:
4-N-Boc-3-piperazinecarboxylic acid is a white crystalline solid with a molecular weight of 215.24g/mol. It can be stable at room temperature. The compound has strong acidity.

Use:
4-N-Boc-3-piperazinecarboxylic acid is widely used in organic synthesis. It can be used as an intermediate in the synthesis of other organic compounds, such as key intermediates in the synthesis of drugs and pesticides. It can also be used in the synthesis of other amide compounds.

Preparation Method:
The preparation of 4-N-Boc-3-piperazinecarboxylic acid generally involves two steps. First, piperazine is reacted with isocyanate to introduce a protecting group (tert-butoxycarbonyl) to form N-tert-Boc-3-piperazine-carboxylic acid isocyanurate. The isocyanate is then converted to the target 4-N-Boc-3-piperazinecarboxylic acid by a hydrolysis reaction.

Safety Information:
The safety of 4-N-Boc-3-piperazinecarboxylic acid has not been fully studied, so relevant safety procedures should be followed when using it. It may cause irritation to the skin, eyes and respiratory system, so it is recommended to wear personal protective equipment to avoid direct contact. In addition, the compound should be stored and handled properly to avoid contact with flammable substances, oxidizing agents and strong acids and bases to reduce safety risks.

Last Update：2024-04-09 21:01:54