Indole-3-acetamide - CAS 879-37-8
Catalog: |
BB038689 |
Product Name: |
Indole-3-acetamide |
CAS: |
879-37-8 |
Synonyms: |
2-(1H-indol-3-yl)acetamide |
IUPAC Name: | 2-(1H-indol-3-yl)acetamide |
Description: | Indole-3-acetamide (CAS# 879-37-8) is a compound that is converted to indole-3-acetic acid by indole-3-acetamide hydrolase in auxin biosynthesis in plants. |
Molecular Weight: | 174.20 |
Molecular Formula: | C10H10N2O |
Canonical SMILES: | C1=CC=C2C(=C1)C(=CN2)CC(=O)N |
InChI: | InChI=1S/C10H10N2O/c11-10(13)5-7-6-12-9-4-2-1-3-8(7)9/h1-4,6,12H,5H2,(H2,11,13) |
InChI Key: | ZOAMBXDOGPRZLP-UHFFFAOYSA-N |
Boiling Point: | 469.7 °C at 760 mmHg |
Melting Point: | 148-150 °C |
Purity: | > 98.0 % (LC) |
Density: | 1.285 g/cm1.285 g/cm3 |
Solubility: | 1.344e+004 mg/L at 25 °C (est) |
Appearance: | White to off white crystalline powder |
MDL: | MFCD00005641 |
LogP: | 1.89600 |
Publication Number | Title | Priority Date |
CN-113462606-A | Strain for preventing infant from diarrhea caused by supplementary food and application thereof | 20210727 |
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-111620837-A | Cedar ketone thiazole amide compound, and preparation method and application thereof | 20200629 |
PMID | Publication Date | Title | Journal |
33002526 | 20201101 | Indole microbial intestinal metabolites expand the repertoire of ligands and agonists of the human pregnane X receptor | Toxicology letters |
25583978 | 20150301 | Hydrazidase, a novel amidase signature enzyme that hydrolyzes acylhydrazides | Journal of bacteriology |
22750991 | 20120701 | Structural studies on ligand-DNA systems: A robust approach in drug design | Journal of biosciences |
22447967 | 20120501 | The pathway of auxin biosynthesis in plants | Journal of experimental botany |
22834303 | 20120501 | [Auxin synthesis by the higher fungus Lentinus edodes (Berk.) Sing in the presence of low concentrations of indole compounds] | Prikladnaia biokhimiia i mikrobiologiia |
Complexity: | 205 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 174.079312947 |
Formal Charge: | 0 |
Heavy Atom Count: | 13 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 174.079312947 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 58.9 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.8 |
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