alpha-Methyl-L-proline
H-.alpha.-Me-Pro-OH
CAS: 42856-71-3
Molecular Formula: C6H11NO2
alpha-Methyl-L-proline - Names and Identifiers
| Name | H-.alpha.-Me-Pro-OH |
| Synonyms | 2-methylproline 2-methyl-D-proline α-methyl-l-proline 5-Methyl-L-Proline (S)-2-Methylproline H-.alpha.-Me-Pro-OH (S)-2-Methyl proline alpha-Methyl-L-proline L-Proline, 2-methyl- (9CI) (2S)-2-methylpyrrolidinium-2-carboxylate (S)-2-methylpyrrolidine-2-carboxylic acid (2S)-2-Methylpyrrolidin-2-ylcarboxylic acid (2s,5s)-5-Methylpyrrolidine-2-Carboxylic Acid |
| CAS | 42856-71-3 |
| EINECS | 610-068-9 |
| InChI | InChI=1/C6H11NO2/c1-6(5(8)9)3-2-4-7-6/h7H,2-4H2,1H3,(H,8,9)/t6-/m1/s1 |
alpha-Methyl-L-proline - Physico-chemical Properties
| Molecular Formula | C6H11NO2 |
| Molar Mass | 129.16 |
| Density | 1.119±0.06 g/cm3(Predicted) |
| Melting Point | 310°C(lit.) |
| Boling Point | 241.9±33.0 °C(Predicted) |
| Flash Point | 100.1°C |
| Solubility | soluble in Methanol |
| Vapor Presure | 0.0116mmHg at 25°C |
| Appearance | powder to crystal |
| Color | White to Almost white |
| BRN | 4350211 |
| pKa | 2.44±0.20(Predicted) |
| Storage Condition | Keep in dark place,Inert atmosphere,2-8°C |
| Refractive Index | 1.475 |
| MDL | MFCD01318647 |
| Use | This product is for scientific research only and shall not be used for other purposes. |
alpha-Methyl-L-proline - Risk and Safety
| Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 29339900 |
alpha-Methyl-L-proline - Introduction
H-.alpha.-Me-Pro-OH(H-.alpha.-Me-Pro-OH) is an organic compound that is an isomer of alpha-amino acids. Its chemical formula is C6H11NO2 and its relative molecular mass is 129.16.
Nature:
H-.alpha.-Me-Pro-OH is a colorless crystal, soluble in water and some organic solvents. It is a chiral molecule and exists in a mixture of two enantiomers.
Use:
H-.alpha.-Me-Pro-OH is commonly used as an intermediate in organic synthesis for the synthesis of drugs, bioactive molecules and polymer materials. Its chiral nature also makes it of great significance in the field of medicine.
Preparation Method:
H-.alpha.-Me-Pro-OH can be synthesized in a variety of ways. A common preparation method is to react 2-bromopropionic acid and glycine, and then selectively synthesize H-.alpha.-Me-Pro-OH through the synthesis step of chiral compounds.
Safety Information:
H-.alpha.-Me-Pro-OH is relatively stable under normal conditions, but may decompose in the presence of high temperatures, sunlight, and oxidants. It is less toxic, but still need to pay attention to prevent inhalation, contact with skin and eyes.
In general, H-.alpha.-Me-Pro-OH is an organic compound with important chemical properties and application value, and can be used safely under correct operation.
Nature:
H-.alpha.-Me-Pro-OH is a colorless crystal, soluble in water and some organic solvents. It is a chiral molecule and exists in a mixture of two enantiomers.
Use:
H-.alpha.-Me-Pro-OH is commonly used as an intermediate in organic synthesis for the synthesis of drugs, bioactive molecules and polymer materials. Its chiral nature also makes it of great significance in the field of medicine.
Preparation Method:
H-.alpha.-Me-Pro-OH can be synthesized in a variety of ways. A common preparation method is to react 2-bromopropionic acid and glycine, and then selectively synthesize H-.alpha.-Me-Pro-OH through the synthesis step of chiral compounds.
Safety Information:
H-.alpha.-Me-Pro-OH is relatively stable under normal conditions, but may decompose in the presence of high temperatures, sunlight, and oxidants. It is less toxic, but still need to pay attention to prevent inhalation, contact with skin and eyes.
In general, H-.alpha.-Me-Pro-OH is an organic compound with important chemical properties and application value, and can be used safely under correct operation.
Last Update：2024-04-09 21:32:41
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