O4-benzyl O1-tert-butyl (2R)-2-methylpiperazine-1,4-dicarboxylate - Names and Identifiers
Name | (R)-2-METHYL-PIPERAZINE-1,4-DICARBOXYLIC ACID 4-BENZYL ESTER 1-TERT-BUTYL ESTER
|
Synonyms | R-1-BOC-4-CBZ-2-METHYLPIPERAZINE (R)-4-Benzyl 1-Boc-2-Methylpiperazine-4-carboxylate O4-benzyl O1-tert-butyl (2R)-2-methylpiperazine-1,4-dicarboxylate (R)-2-METHYL-PIPERAZINE-1,4-DICARBOXYLIC ACID 4-BENZYL ESTER 1-TERT-BUTYL ESTER 2-methylpiperazine-1,4-dicarboxylic acid O1-tert-butyl ester O4-(phenylmethyl) ester 1,4-Piperazinedicarboxylic acid, 2-methyl-, 1-(1,1-dimethylethyl) 4-(phenylmethyl) ester
|
CAS | 128102-16-9
|
InChI | InChI=1/C18H26N2O4/c1-14-12-19(10-11-20(14)17(22)24-18(2,3)4)16(21)23-13-15-8-6-5-7-9-15/h5-9,14H,10-13H2,1-4H3/t14-/m1/s1 |
O4-benzyl O1-tert-butyl (2R)-2-methylpiperazine-1,4-dicarboxylate - Physico-chemical Properties
Molecular Formula | C18H26N2O4
|
Molar Mass | 334.41 |
Density | 1.137g/cm3 |
Boling Point | 435.4°C at 760 mmHg |
Flash Point | 217.1°C |
Vapor Presure | 8.81E-08mmHg at 25°C |
Storage Condition | 2-8°C |
Refractive Index | 1.527 |
O4-benzyl O1-tert-butyl (2R)-2-methylpiperazine-1,4-dicarboxylate - Introduction
(R)-1-Boc-4-Cbz-2-methylpiperazine is an organic compound with the following properties:
1. Appearance:(R)-1-Boc-4-Cbz-2-methylpiperazine is a white or off-white solid.
2. molecular formula: C18H23N3O3
3. Solubility: It has good solubility in common organic solvents, such as methanol, ethanol and dichloromethane.
4. Uses:(R)-1-Boc-4-Cbz-2-methyl piperazine is an important intermediate compound, commonly used in organic synthesis. It can be used to synthesize biologically active molecules, such as drugs, pesticides and dyes. It can also be used in the synthesis of chiral compounds, natural products and materials, etc.
5. Preparation Method:(R)-1-Boc-4-Cbz-2-methylpiperazine can be prepared by an existing chemical synthesis method. A common method is obtained by reacting (Boc)2O and di (benzyloxy) methyl carbonate with 2-methylpiperazine in a suitable solvent. (R)-1-Boc-4-Cbz-2-methylpiperazine is then prepared by appropriate structural modification reactions, for example using reducing agents of the benzamic acid protecting group.
Last Update:2024-04-09 18:58:34