3-(3-Indolyl)-2-oxopropanoic Acid - CAS 392-12-1
Catalog: |
BB023890 |
Product Name: |
3-(3-Indolyl)-2-oxopropanoic Acid |
CAS: |
392-12-1 |
Synonyms: |
3-(1H-indol-3-yl)-2-oxopropanoic acid; 3-(1H-indol-3-yl)-2-oxopropanoic acid |
IUPAC Name: | 3-(1H-indol-3-yl)-2-oxopropanoic acid |
Description: | 3-(3-Indolyl)-2-oxopropanoic Acid (CAS# 392-12-1) is a compound involved in the biosynthesis of Indole-3-acetic acid, a plant hormone which plays important roles in regulating growth and responses to environmental changes. |
Molecular Weight: | 203.19 |
Molecular Formula: | C11H9NO3 |
Canonical SMILES: | C1=CC=C2C(=C1)C(=CN2)CC(=O)C(=O)O |
InChI: | InChI=1S/C11H9NO3/c13-10(11(14)15)5-7-6-12-9-4-2-1-3-8(7)9/h1-4,6,12H,5H2,(H,14,15) |
InChI Key: | RSTKLPZEZYGQPY-UHFFFAOYSA-N |
Boiling Point: | 445.2 °C at 760 mmHg |
Density: | 1.421 g/cm3 |
MDL: | MFCD00005640 |
LogP: | 1.36410 |
Publication Number | Title | Priority Date |
CN-113073066-A | Lactobacillus reuteri and application, composition, medicine and food thereof | 20210416 |
CN-112481173-A | Bacillus endophyticus GBW-F008 for producing indoleacetic acid and application thereof | 20201221 |
CN-112553230-A | High-yield IAA trichoderma viride engineering strain and construction method and application thereof | 20201221 |
CN-112553230-B | High-yield IAA trichoderma viride engineering strain and construction method and application thereof | 20201221 |
CN-112300109-A | Fluorene antibiotic, preparation method thereof and application thereof in preparation of antitumor drugs and enzyme inhibitors | 20201015 |
PMID | Publication Date | Title | Journal |
26686552 | 20160119 | Evidence for New Light-Independent Pathways for Generation of the Endogenous Aryl Hydrocarbon Receptor Agonist FICZ | Chemical research in toxicology |
23114508 | 20121101 | [Pityriasis versicolor : new aspects of an old disease] | Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete |
22924530 | 20121001 | Indole derivative production by the root endophyte Piriformospora indica is not required for growth promotion but for biotrophic colonization of barley roots | The New phytologist |
22883136 | 20120810 | Protocol: High-throughput and quantitative assays of auxin and auxin precursors from minute tissue samples | Plant methods |
22573801 | 20120701 | Biosynthesis of the halogenated auxin, 4-chloroindole-3-acetic acid | Plant physiology |
Complexity: | 277 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 203.058243149 |
Formal Charge: | 0 |
Heavy Atom Count: | 15 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 203.058243149 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 70.2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.3 |
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