(2S)-2-(氨基羰基)-2,3-二氢-1H-吡咯-1-甲酸叔丁基酯 - Names and Identifiers
Name | tert-butyl (2S)-2-carbamoyl-2,3-dihydro-1H-pyrrole-1-carboxylate
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Synonyms | Saxaint-T Saxagliptin impurity I (S)-Boc-2-carbaMoyl-2,3-dihydro-1H-pyrrole (S)-tert-butyl 2-carbaMoyl-2,3-dihydropyrrole-1-carboxylate tert-butyl (S)-2-carbamoyl-2,3-dihydro-1H-pyrrole-1-carboxylate (S)-tert-Butyl 2-carbamoyl-2,3-dihydro-1H-pyrrole-1-carboxylate tert-butyl (2S)-2-carbamoyl-2,3-dihydro-1H-pyrrole-1-carboxylate tert-Butyl (2S)-2-carbamoyl-2,3-dihydro-1H-pyrrole-1-carboxylate (2S)-2-(Aminocarbonyl)-2,3-dihydro-1H-pyrrole-1-carboxylic acid 1,1-dimethylethyl ester 1H-pyrrole-1-carboxylic acid, 2-(aminocarbonyl)-2,3-dihydro-, 1,1-dimethylethyl ester, (2S)- 1H-Pyrrole-1-carboxylic acid, 2-(aMinocarbonyl)-2,3-dihydro-, 1,1-diMethylethyl ester, (2S)-
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CAS | 709031-38-9
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EINECS | 615-204-0 |
InChI | InChI=1/C10H16N2O3/c1-10(2,3)15-9(14)12-6-4-5-7(12)8(11)13/h4,6-7H,5H2,1-3H3,(H2,11,13)/t7-/m0/s1 |
(2S)-2-(氨基羰基)-2,3-二氢-1H-吡咯-1-甲酸叔丁基酯 - Physico-chemical Properties
Molecular Formula | C10H16N2O3
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Molar Mass | 212.25 |
Density | 1.187±0.06 g/cm3(Predicted) |
Boling Point | 386.5±42.0 °C(Predicted) |
Flash Point | 187.525°C |
Vapor Presure | 0mmHg at 25°C |
pKa | 15.57±0.20(Predicted) |
Storage Condition | 2-8°C |
Refractive Index | 1.523 |
(2S)-2-(氨基羰基)-2,3-二氢-1H-吡咯-1-甲酸叔丁基酯 - Introduction
tert-butyl (2S)-2-carbamoyl-2 is an organic compound with the following chemical structure:
Its molecular formula is C12H20N2O3 and its relative molecular mass is 240.3.
Nature:
tert-butyl (2S)-2-carbamoyl-2 is a solid, soluble in organic solvents such as methanol and dichloromethane. It has a relatively low melting and boiling point and is usually a solid at room temperature.
Use:
tert-butyl (2S)-2-carbamoyl-2, is an intermediate compound widely used in organic synthesis. It can be used in the synthesis of biologically active compounds such as pharmaceuticals and pesticides.
Preparation Method:
tert-butyl (2S)-2-carbamoyl-2, can be prepared by reacting N-protected methylpyrrolamine and tert-butyl methacrylate in an anhydrous solvent. The reaction generally requires the use of a catalyst and a suitable solvent. The specific reaction conditions of the preparation process can be adjusted and optimized according to specific experimental requirements.
Safety Information:
In the process of use and preservation, attention should be paid to correct experimental operation and safe operation. Dust or liquid of the compound may cause irritation to the eyes, skin, respiratory tract, etc. Therefore, when operating, wear appropriate personal protective equipment, such as laboratory gloves, goggles and respiratory protection. During storage, it should be placed in a dry, cool place and avoid contact with oxidants or flammable materials.
Last Update:2024-04-09 21:21:28