Indole-3-carboxaldehyde
CAS No. 487-89-8
Indole-3-carboxaldehyde ( 3-Formylindole )
Catalog No. M21421 CAS No. 487-89-8
1H-Indole-3-carboxaldehyde also known as 3-formylindole or 3-indolealdehyde belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety which consists of pyrrole ring fused to benzene to form 23-benzopyrrole.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
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Biological Information
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Product NameIndole-3-carboxaldehyde
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NoteResearch use only not for human use.
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Brief Description1H-Indole-3-carboxaldehyde also known as 3-formylindole or 3-indolealdehyde belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety which consists of pyrrole ring fused to benzene to form 23-benzopyrrole.
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Description1H-Indole-3-carboxaldehyde also known as 3-formylindole or 3-indolealdehyde belongs to the class of organic compounds known as indoles. Indoles are compounds containing an indole moiety which consists of pyrrole ring fused to benzene to form 23-benzopyrrole. 1H-Indole-3-carboxaldehyde is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body 1H-Indole-3-carboxaldehyde has been detected but not quantified in several different foods such as gram beans brussel sprouts cucumbers cereals and cereal products and white cabbages. This could make 1H-indole-3-carboxaldehyde a potential biomarker for the consumption of these foods. A heteroarenecarbaldehyde that is indole in which the hydrogen at position 3 has been replaced by a formyl group.
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Synonyms3-Formylindole
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PathwayProteasome/Ubiquitin
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TargetEndogenous Metabolite
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RecptorHuman Endogenous Metabolite
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Research Area——
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Indication——
Chemical Information
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CAS Number487-89-8
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Formula Weight145.16
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Molecular FormulaC9H7NO
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Purity>98% (HPLC)
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SolubilityDMSO:2 mg/mL (137.78 mM)
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SMILESO=Cc1c[nH]c2c1cccc2
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Robert E. Stutz et al. Enzymatic Formation of Indole-3-Carboxaldehyde from Indole-3-Acetic Acid. Plant Physiol. 1958 May; 33(3): 207–212.
molnova catalog
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