| Weight | 218.256 g/mol |
|---|---|
| Formula | C12H14N2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
N-Methyl-L-tryptophan (526-31-8)
abrine
Score:
#2595 in Biochemistry
,
#6460 in Chemistry
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- Sigma-Aldrich - N-Methyl-L-tryptophan49.40 - 117.00 USD
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- Chiral ligands derived from abrine. Part 6: Importance of a bulky N-alkyl group in indole-containing chiral beta-tertiary amino alcohols for controlling enantioselectivity in addition of diethylzinc toward aldehydes (Tetrahedron-asymmetry, 2000)
- Chiral ligands derived from Abrine 8. An experimental and theoretical study of free ligand conformational preferences and the addition of diethylzinc to benzaldehyde. (Journal of Organic Chemistry, 2005)
- Chiral ligands derived from Abrine .2. Oxazolidines as promoters for enantioselective addition of diethylzinc toward aromatic aldehydes (Tetrahedron-asymmetry, 1996)
- Acyl-Enzyme Intermediates in the -Chymotrypsin-Catalyzed Hydrolysis of Specific Substrates. the Relative Rates of Hydrolysis of Ethyl, Methyl andp-Nitrophenyl Esters of N-Acetyl-L-Tryptophan (Journal of the American Chemical Society, 1963)
- Chiral ligands derived from abrine. 1. Synthesis of sec- and tert--amino alcohols and catalysis for enantioselective addition of diethylzinc toward aromatic aldehydes (Tetrahedron-asymmetry, 1995)
- Chiral ligands derived from Abrine .3. Asymmetric Pictet-Spengler reaction of Abrine methyl ester and synthesis of chiral 1,2,3,4-tetrahydro-beta-carbolines as promoters in addition of diethylzinc toward aromatic aldehydes (Tetrahedron Letters, 1996)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - abrine
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SMILESCNC(CC1=CNC2=CC=CC=C21)C(=O)O
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InChIKeyCZCIKBSVHDNIDH-UHFFFAOYSA-N
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N-Methyl-L-tryptophan
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