L-Tryptophanamide hydrochloride

• CAS: 5022-65-1
• Catalog Number: ACM5022651
• Category: Other Products
• Molecular Weight: 239.7
• Molecular Formula: C11H14ClN3O
• Synonyms: Tryptophanamide oxalate
• IUPAC Name: (2S)-2-Amino-3-(1H-indol-3-yl)propanamide;hydrochloride
• SMILES: C1=CC=C2C(=C1)C(=CN2)CC(C(=O)N)N.Cl
• InChI: InChI=1S/C11H13N3O.ClH/c12-9(11(13)15)5-7-6-14-10-4-2-1-3-8(7)10;/h1-4,6,9,14H,5,12H2,(H2,13,15);1H/t9-;/m0./s1
• InChI Key: WOBDANBSEWOYKN-FVGYRXGTSA-N
• Boiling Point: 498.7 °C/760 mmHg
• Melting Point: 250 °C
• Flash Point: 255.4 °C
• Appearance: White to off-white solid
• Storage: Inert atmosphere, room temperature
• Complexity: 244
• Exact Mass: 239.0825398
• Isomeric SMILES: C1=CC=C2C(=C1)C(=CN2)C[C@@H](C(=O)N)N.Cl
• Monoisotopic Mass: 239.0825398
• Topological Polar Surface Area: 84.9 Ų

Synthetic Use

Upstream Synthesis Route 1

• 62549-92-2

• 5022-65-1

Reference: [1] Patent: WO2018/33724, 2018, A1, . Location in patent: Page/Page column 50

Upstream Synthesis Route 2

• 20696-64-4

• 5022-65-1

Reference: [1] Journal of Medicinal Chemistry, 2003, vol. 46, # 7, p. 1191 - 1203

Upstream Synthesis Route 3

• 7432-21-5

• 5022-65-1

Reference: [1] Journal of Medicinal Chemistry, 2003, vol. 46, # 7, p. 1191 - 1203

Upstream Synthesis Route 4

• 6159-33-7

• 5022-65-1

Reference: [1]Chemische Berichte,1983,vol. 116,p. 2037 - 2040

Downstream Synthesis Route 1

• 5022-65-1
• 130581-71-4

• 130581-68-9

Reference: [1]Bulletin of the Polish Academy of Sciences: Chemistry,1989,vol. 37,p. 331 - 338

* For details of the synthesis route, please refer to the original source to ensure accuracy.