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Chemical Structure| 3913-67-5 Chemical Structure| 3913-67-5
Chemical Structure| 3913-67-5

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N-Me-Ala-OH is a derivative of alanine, widely used in peptide synthesis. Its methylated structure helps enhance peptide stability and influences protein-protein interactions.

Synonyms: H-N-Me-Ala-OH

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Product Details of N-Me-Ala-OH

CAS No. :3913-67-5
Formula : C4H9NO2
M.W : 103.12
SMILES Code : C[C@H](NC)C(O)=O
Synonyms :
H-N-Me-Ala-OH
MDL No. :MFCD00037241
InChI Key :GDFAOVXKHJXLEI-VKHMYHEASA-N
Pubchem ID :5288725

Safety of N-Me-Ala-OH

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of N-Me-Ala-OH

* 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.

  • Downstream synthetic route of [ 3913-67-5 ]

[ 3913-67-5 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 15761-39-4 ]
  • [ 13734-41-3 ]
  • [ 13139-15-6 ]
  • [ 3913-67-5 ]
  • [ 3060-46-6 ]
  • [ 2480-93-5 ]
  • [ 18942-49-9 ]
  • C59H94N12O10 [ No CAS ]
  • 2
  • [ 15761-39-4 ]
  • [ 13734-41-3 ]
  • [ 13139-15-6 ]
  • [ 3913-67-5 ]
  • [ 3060-46-6 ]
  • [ 2480-93-5 ]
  • [ 18942-49-9 ]
  • C60H94N12O10 [ No CAS ]
  • 3
  • jahanyne [ No CAS ]
  • [ 3913-67-5 ]
  • [ 2480-23-1 ]
  • [ 2566-30-5 ]
  • [ 147-85-3 ]
  • 4
  • urumamide [ No CAS ]
  • [ 3913-67-5 ]
  • [ 72-18-4 ]
  • [ 17407-56-6 ]
  • [ 2480-23-1 ]
  • [ 61-90-5 ]
  • [ 3060-46-6 ]
  • [ 4125-98-8 ]
  • [ 147-85-3 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In water; at 110℃; for 24h; Urumamide (1) (0.7 mg) was treated with 9 N HCl (100 L) for 24 h at 110 C. The hydrolyzed product was evaporated to dryness and could be separated into each component by HPLC. [Cosmosil 5C18-PAQ (4.6 × 250 mm); flowrate, 1.0 mL/min; detection at 215 nm; solvent H2O. Retention times (min) of components: N-Me-Ala (tR = 3.0 min), Pro(tR = 3.2 min), Val (tR = 3.4 min), N-Me-Val (tR = 3.7 min), Leu (tR = 4.8 min), N-Me-Ile (tR = 5.3 min), N-Me-Leu (tR =6.0 min)].
  • 5
  • janadolide [ No CAS ]
  • [ 3913-67-5 ]
  • [ 72-18-4 ]
  • [ 3060-46-6 ]
  • [ 147-85-3 ]
  • 6
  • cyclombandakamine A<SUB>1</SUB> [ No CAS ]
  • [ 56-41-7 ]
  • [ 338-69-2 ]
  • [ 3775-72-2 ]
  • [ 3775-73-3 ]
  • [ 3913-67-5 ]
  • [ 29475-64-7 ]
  • (S)-3-(N-methylamino)butanoic acid [ No CAS ]
  • (R)-N-methyl-3-aminobutyric acid [ No CAS ]
  • 7
  • cyclombandakamine A<SUB>2</SUB> [ No CAS ]
  • [ 56-41-7 ]
  • [ 338-69-2 ]
  • [ 3775-72-2 ]
  • [ 3775-73-3 ]
  • [ 3913-67-5 ]
  • [ 29475-64-7 ]
  • (S)-3-(N-methylamino)butanoic acid [ No CAS ]
  • (R)-N-methyl-3-aminobutyric acid [ No CAS ]
 

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