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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
N-DL-Me-Ala-OH is a methylated alanine derivative, commonly used in polypeptide synthesis, enhancing stability and modulating cellular metabolism.
Synonyms: H-N-Me-DL-Ala-OH; N-Methyl-DL-alanine
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Batch number can be found on the product's label following the word 'Batch'.
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CAS No. : | 600-21-5 |
Formula : | C4H9NO2 |
M.W : | 103.12 |
SMILES Code : | CC(NC)C(O)=O |
Synonyms : |
H-N-Me-DL-Ala-OH; N-Methyl-DL-alanine
|
MDL No. : | MFCD00063136 |
InChI Key : | GDFAOVXKHJXLEI-UHFFFAOYSA-N |
Pubchem ID : | 4377 |
GHS Pictogram: |
![]() |
Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P305+P351+P338 |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
61% | With lithium aluminium tetrahydride; In tetrahydrofuran; at 70℃; for 16h; | To a solution of 2-(methylamino)propanoic acid (10.0 g, 96.97 mmol) in THF (200 mL) wasadded LiAIH4 (5.52 g, 145.46 mmol) portionwise. The mixture was heated to 70 C for 16 h.After cooling the reaction to room temperature, water (10 mL) was added. The mixture was filtered and concentrated in vacuo. The crude residue was washed with HCI/EtOAc (2 M, 50 mL) to give the title compound (5.3 g, 61%) as a brown oil that required no fartherpurification. ?H NMR (400 MHz, CD3OD) 6 3.81 - 3.78 (m, 1H), 3.56 - 3.51 (m, IH), 3.26 -3.22 (m, IH), 2.68 (s, 3H), 1.28 (d,J= 7.2 Hz, 3H). |