Structure

Boc-6-fluoro-DL-tryptophan

CAS
67308-25-2
Catalog Number
ACM67308252-1
Category
Amino Acids
Molecular Weight
322.3
Molecular Formula
C16H19FN2O4

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Specification

Description
(S)-2-((tert-Butoxycarbonyl)amino)-3-(6-fluoro-1H-indol-3-yl)propanoic acid is a synthetic amino acid derivative with the chemical formula C19H24FN3O5. It is a prodrug for indole-3-acetic acid, a plant hormone that is involved in plant growth and development
Synonyms
(S)-2-((tert-Butoxycarbonyl)amino)-3-(6-fluoro-1H-indol-3-yl)propanoic acid
IUPAC Name
(2S)-3-(6-fluoro-1H-indol-3-yl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Canonical SMILES
CC(C)(C)OC(=O)NC(CC1=CNC2=C1C=CC(=C2)F)C(=O)O
InChI
1S/C16H19FN2O4/c1-16(2,3)23-15(22)19-13(14(20)21)6-9-8-18-12-7-10(17)4-5-11(9)12/h4-5,7-8,13,18H,6H2,1-3H3,(H,19,22)(H,20,21)/t13-/m0/s1
InChI Key
VVTAJUCNHDSAJU-ZDUSSCGKSA-N
Boiling Point
538.3±50.0 ℃at 760 mmHg
Flash Point
279.3±30.1 ℃
Density
1.3±0.1 g/cm3
Application
(S)-2-((tert-Butoxycarbonyl)amino)-3-(6-fluoro-1H-indol-3-yl)propanoic acid has potential applications in various scientific experiments, including plant growth regulation, cancer research, and drug development. The compound can be used as a prodrug for indole-3-acetic acid in plant growth studies, and its growth-promoting effects could be useful in the development of new plant growth regulators. In cancer research, the compound's inhibition of cancer cell growth could be valuable in the discovery of new anticancer agents.
Exact Mass
322.132874
Functional Group
Boc
LogP
2.94
MDL Number
MFCD02682360
PSA
91.42
Refractive Index
1.59
Storage Temperature
4 ℃
Type
Unusual Amino Acids, Analogs of Tryptophan
Vapor Pressure
0.0±1.5 mmHg at 25℃
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