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Saxagliptin impurity I

tert-butyl (2S)-2-carbamoyl-2,3-dihydro-1H-pyrrole-1-carboxylate

CAS: 709031-38-9

Molecular Formula: C10H16N2O3

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Saxagliptin impurity I - Names and Identifiers

Name tert-butyl (2S)-2-carbamoyl-2,3-dihydro-1H-pyrrole-1-carboxylate
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)-
CAS 709031-38-9
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

Saxagliptin impurity I - Physico-chemical Properties

Molecular FormulaC10H16N2O3
Molar Mass212.25
Density1.187±0.06 g/cm3(Predicted)
Boling Point386.5±42.0 °C(Predicted)
Flash Point187.525°C
Vapor Presure0mmHg at 25°C
pKa15.57±0.20(Predicted)
Storage Condition2-8°C
Refractive Index1.523

Saxagliptin impurity I - 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
Saxagliptin impurity I
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