Indole-3-carboxaldehyde-13C

Modify Date: 2025-09-18 11:06:16

Indole-3-carboxaldehyde-13C structure	Common Name	Indole-3-carboxaldehyde-13C
	CAS Number	1093452-52-8	Molecular Weight	146.15
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₈₁₃CH₇NO	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of Indole-3-carboxaldehyde-13C

Indole-3-carboxaldehyde-13C (3-Formylindole-13C) is a 13C labeled Indole-3-carboxaldehyde (HY-W007376). Indole-3-carboxaldehyde (3-Formylindole), a banlangen extract, is the product of the oxidative degradation of indole-3-acetic acid (IAA) by crude enzyme preparations from etiolated pea seedlings. Indole-3-carboxaldehyde (3-Formylindole) is a biochemical used to prepare analogs of the indole phytoalexin cyclobrassinin[1][2].

Name	1H-indole-3-carbaldehyde-13C
Synonym	More Synonyms

Description	Indole-3-carboxaldehyde-13C (3-Formylindole-13C) is a 13C labeled Indole-3-carboxaldehyde (HY-W007376). Indole-3-carboxaldehyde (3-Formylindole), a banlangen extract, is the product of the oxidative degradation of indole-3-acetic acid (IAA) by crude enzyme preparations from etiolated pea seedlings. Indole-3-carboxaldehyde (3-Formylindole) is a biochemical used to prepare analogs of the indole phytoalexin cyclobrassinin[1][2].
Related Catalog	Research Areas >> Others
References	[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-246. [2]. Robert E. Stutz, et al. Enzymatic Formation of Indole-3-Carboxaldehyde from Indole-3-Acetic Acid. Plant Physiol. 1958 May; 33(3): 207–212.

Description

Related Catalog

Research Areas >> Others

References

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-246.

[2]. Robert E. Stutz, et al. Enzymatic Formation of Indole-3-Carboxaldehyde from Indole-3-Acetic Acid. Plant Physiol. 1958 May; 33(3): 207–212.