Molecular structure of 3-Indoleacetonitrile, CAS Number: 771-51-7
3-Indoleacetonitrile (CAS 771-51-7)
Alternate Names:
(3-Indolyl)acetonitrile; 3-(Cyanomethyl)indole
Application:
3-Indoleacetonitrile is a plant growth activator
CAS Number:
771-51-7
Purity:
≥97%
Molecular Weight:
156.18
Molecular Formula:
C10H8N2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
3-Indoleacetonitrile functions as a precursor in the synthesis of various indole derivatives. It acts as a key intermediate in the production of indole-3-acetic acid. 3-Indoleacetonitrile serves as a starting material for the synthesis of biologically active compounds in the experimental. Its mechanism of action involves undergoing chemical transformations to yield indole-3-acetic acid or other indole-based molecules.
3-Indoleacetonitrile (CAS 771-51-7) References
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- Gas chromatography-mass spectrometry evidence for several endogenous auxins in pea seedling organs. | Schneider, EA., et al. 1985. Planta. 165: 232-41. PMID: 24241048
- Normal pregnancy induced glucose metabolic stress in a longitudinal cohort of healthy women: Novel insights generated from a urine metabolomics study. | Wang, M., et al. 2018. Medicine (Baltimore). 97: e12417. PMID: 30290597
- Urinary metabolomics reveals novel interactions between metal exposure and amino acid metabolic stress during pregnancy. | Wang, M., et al. 2018. Toxicol Res (Camb). 7: 1164-1172. PMID: 30510686
- Dynamic metabolic profiles of the marine macroalga Ulva prolifera during fragmentation-induced proliferation. | He, Y., et al. 2019. PLoS One. 14: e0214491. PMID: 31091237
- Urinary metabolites identified using metabolomic analysis as potential biomarkers of nocturia in elderly men. | Kira, S., et al. 2020. World J Urol. 38: 2563-2569. PMID: 31797073
- Antibiofilm and Antivirulence Properties of Indoles Against Serratia marcescens. | Sethupathy, S., et al. 2020. Front Microbiol. 11: 584812. PMID: 33193228
- The indole alkaloids from the roots of Isatidis Radix. | Wang, F., et al. 2021. Fitoterapia. 153: 104950. PMID: 34089787
- 3-Indoleacetonitrile Is Highly Effective in Treating Influenza A Virus Infection In Vitro and In Vivo. | Zhao, X., et al. 2021. Viruses. 13: PMID: 34452298
- Potential Targets for Overactive Bladder in Older Men Based on Urinary Analysis of Metabolomics. | Kira, S., et al. 2022. Urol Int. 106: 672-678. PMID: 34569539
- 3-indoleacetonitrile attenuates biofilm formation and enhances sensitivity to imipenem in Acinetobacter baumannii. | Kashyap, S., et al. 2022. Pathog Dis. 80: PMID: 35867872
- In vitro and in vivo effects of 3-indoleacetonitrile-A potential new broad-spectrum therapeutic agent for SARS-CoV-2 infection. | Hui, X., et al. 2023. Antiviral Res. 209: 105465. PMID: 36402240
- Carbon and nitrogen metabolism affects kentucky bluegrass rhizome expansion. | Ran, F., et al. 2023. BMC Plant Biol. 23: 221. PMID: 37101108
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NIT1.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-Indoleacetonitrile, 5 g | sc-256518 | 5 g | $60.00 |