Indole-3-acetaldehyde

Names
Preferred IUPAC name

(1H-Indol-3-yl)acetaldehyde

Other names

Indoleacetaldehyde; 1H-Indole-3-acetaldehyde; 2-(Indol-3-yl)acetaldehyde; Indole-3-acetaldehyde; Indoleacetaldehyde; 1H-Indol-3-ylacetaldehyde; 2-(3-Indolyl)acetaldehyde; Indol-3-ylacetaldehyde; Tryptaldehyde

Identifiers

CAS Number

* 2591-98-2

3D model (JSmol)

* Interactive image

ChEBI |

* CHEBI:18086

ChemSpider |

* 778

KEGG |

* C00637

MeSH | C001655

PubChem CID

* 800

UNII |

* A346H8E8WU Y

InChI

* InChI=1S/C10H9NO/c12-6-5-8-7-11-10-4-2-1-3-9(8)10/h1-4,6-7,11H,5H2

Key: WHOOUMGHGSPMGR-UHFFFAOYSA-N

SMILES

* O=CCC1=CNC2=CC=CC=C12

Properties

Chemical formula

| C10H9NO
Molar mass | 159.188 g·mol−1

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Infobox references

Indole-3-acetaldehyde belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole.

Indole-3-acetaldehyde is a substrate for retina-specific copper amine oxidase, aldehyde dehydrogenase X (mitochondrial), amine oxidase B, amiloride-sensitive amine oxidase, aldehyde dehydrogenase (mitochondrial), fatty aldehyde dehydrogenase, 4-trimethylaminobutyraldehyde dehydrogenase, aldehyde dehydrogenase (dimeric NADP-preferring), aldehyde dehydrogenase family 7 member A1, amine oxidase A, aldehyde dehydrogenase 1A3 and membrane copper amine oxidase.[1]

## References

1. ↑ "Indole-3-acetic acid biosynthetic pathways in the basidiomycetous yeast Rhodosporidium paludigenum". Arch Microbiol 198 (5): 429-37. 2016. doi:10.1007/s00203-016-1202-z. https://rd.springer.com/article/10.1007/s00203-016-1202-z.

## External links

* Indoleacetaldehyde (HMDB01190)

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*[CID]: Compound ID