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Structure

L-Tryptophanamide hydrochloride

CAS
5022-65-1
Catalog Number
ACM5022651
Category
Other Products
Molecular Weight
239.7
Molecular Formula
C11H14ClN3O

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Specification

Synonyms
Tryptophanamide oxalate
IUPAC Name
(2S)-2-Amino-3-(1H-indol-3-yl)propanamide;hydrochloride
Canonical 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

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.

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