L-ALANINE METHYLAMIDE HYDROCHLORIDE
N-methyl-L-alaninamide
CAS: 61275-22-7
Molecular Formula: C4H11ClN2O
L-ALANINE METHYLAMIDE HYDROCHLORIDE - Names and Identifiers
| Name | N-methyl-L-alaninamide |
| Synonyms | H-Ala-NHMe H-Ala-Nhme Hcl H-ALA-NHME HCL ALANINE-NHME HCL N-methyl-L-alaninamide L-Alanine methylamide HCl L-ALANINE METHYLAMIDE HYDROCHLORIDE propanamide, 2-amino-N-methyl-, (2S)- L-ALANINE N-METHYLAMIDE HYDROCHLORIDE N~1~-methyl-L-alaninamide hydrochloride (S)-2-AMino-N-MethylpropanaMide hydrochloride |
| CAS | 61275-22-7 |
| InChI | InChI=1/C4H10N2O/c1-3(5)4(7)6-2/h3H,5H2,1-2H3,(H,6,7)/t3-/m0/s1 |
L-ALANINE METHYLAMIDE HYDROCHLORIDE - Physico-chemical Properties
| Molecular Formula | C4H11ClN2O |
| Molar Mass | 138.6 |
| Density | 0.976g/cm3 |
| Melting Point | 218-220 °C(Solv: methanol (67-56-1); ethyl ether (60-29-7)) |
| Boling Point | 257°C at 760 mmHg |
| Flash Point | 109.2°C |
| Vapor Presure | 0.0149mmHg at 25°C |
| Storage Condition | Inert atmosphere,Room Temperature |
| Refractive Index | 1.442 |
L-ALANINE METHYLAMIDE HYDROCHLORIDE - Introduction
N-methyl-L-alaninamide(N-methyl-L-alaninamide) is an organic compound. Its chemical formula is C4H10N2O2 · HCl, and the structure contains an amine group and a methylamide group, where the methylamide group is attached to the alpha carbon on the alanine. It is colorless to pale yellow crystalline, soluble in water and some organic solvents.
N-methyl-L-alaninamide has a wide range of uses in the field of medicine. It can be used as an intermediate in the synthesis of drugs and plays an important role in the synthesis of certain drugs. In addition, it is also applied to organic synthesis reactions such as amination reactions and peptide synthesis reactions. In the research field, it can be used to synthesize small molecule compounds, or as a ligand in metal-catalyzed reactions.
The method for preparing N-methyl-L-alaninamide can be obtained by reacting L-alanine with an acidic solution (such as hydrochloric acid), and then adding formyl chloride for acylation. Finally, the final product is obtained by a crystallization precipitation operation.
Regarding safety information, the toxicity of N-methyl-L-alaninamide is low, but it is still necessary to pay attention to safe operation. Avoid contact with skin and eyes when using, and ensure that the operation is carried out in a well-ventilated place. During storage and handling, contact with oxidants, strong acids and strong bases should be avoided to avoid dangerous reactions.
N-methyl-L-alaninamide has a wide range of uses in the field of medicine. It can be used as an intermediate in the synthesis of drugs and plays an important role in the synthesis of certain drugs. In addition, it is also applied to organic synthesis reactions such as amination reactions and peptide synthesis reactions. In the research field, it can be used to synthesize small molecule compounds, or as a ligand in metal-catalyzed reactions.
The method for preparing N-methyl-L-alaninamide can be obtained by reacting L-alanine with an acidic solution (such as hydrochloric acid), and then adding formyl chloride for acylation. Finally, the final product is obtained by a crystallization precipitation operation.
Regarding safety information, the toxicity of N-methyl-L-alaninamide is low, but it is still necessary to pay attention to safe operation. Avoid contact with skin and eyes when using, and ensure that the operation is carried out in a well-ventilated place. During storage and handling, contact with oxidants, strong acids and strong bases should be avoided to avoid dangerous reactions.
Last Update：2024-04-09 20:52:54
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View History
L-ALANINE METHYLAMIDE HYDROCHLORIDE
1-甲基-5-(哌啶-4-基氧基)-1H-吲唑盐酸盐
Titanium(IV) Bromide
à,à,à,4-tetrafluoro-p-toluoyl chloride
2-(甲氧基羰基)环丙烷羧酸
尼达尼布标准品004
L-CIS/TRANS-CHA(4-NH-ALLOC)
环己烷-12-冠-4-醚
(S)-(-)-6,7-二甲氧基-1,2,3,4-四氢异喹啉-3-羧酸
2-氯-N-[(2-甲氧基苯基)甲基]乙酰胺
1-甲基-5-(哌啶-4-基氧基)-1H-吲唑盐酸盐
Titanium(IV) Bromide
à,à,à,4-tetrafluoro-p-toluoyl chloride
2-(甲氧基羰基)环丙烷羧酸
尼达尼布标准品004
L-CIS/TRANS-CHA(4-NH-ALLOC)
环己烷-12-冠-4-醚
(S)-(-)-6,7-二甲氧基-1,2,3,4-四氢异喹啉-3-羧酸
2-氯-N-[(2-甲氧基苯基)甲基]乙酰胺