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I3750

Sigma-Aldrich

3-Indoleacetic acid

98%

Synonym(s):

Heteroauxin, IAA

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10 MG
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10 MG
CA$1,600.00

About This Item

Empirical Formula (Hill Notation):
C10H9NO2
CAS Number:
87-51-4
Molecular Weight:
175.18
Beilstein:
143358
EC Number:
201-748-2
MDL number:
MFCD00005636
UNSPSC Code:
12352100
PubChem Substance ID:
24896043
NACRES:
NA.22

CA$1,600.00

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Quality Level

200

Assay

98%

mp

165-169 °C (lit.)

SMILES string

OC(=O)Cc1c[nH]c2ccccc12

InChI

1S/C10H9NO2/c12-10(13)5-7-6-11-9-4-2-1-3-8(7)9/h1-4,6,11H,5H2,(H,12,13)

InChI key

SEOVTRFCIGRIMH-UHFFFAOYSA-N

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manufacturer/tradename

Drummond Scientific 5-000-1001-X10

manufacturer/tradename

Drummond Scientific 2-000-001

manufacturer/tradename

Drummond Scientific 5-000-1001-X

manufacturer/tradename

Drummond Scientific 2-000-010

material

glass

material

glass

material

glass

material

glass

packaging

pack of 100 ea

packaging

pack of 1, pack of 250 ea

packaging

pack of 100 ea

packaging

pack of 250 ea

capacity

10 μL

capacity

1-5 μL

capacity

1 - 5 μL

capacity

10 μL

volume range

1-10 μL

volume range

-

volume range

1-5 μL

volume range

-

General description

3-Indoleacetic acid (IAA) is a naturally occurring hydrophilic organic compound consists of an unsaturated aromatic ring that is commonly used in the synthesis of indolylated diarylmethanes, α-acetoxyl ketones, and Indolmethyl-Chromones via copper catalyzed coupling reactions. [1] [2] [3] [4]

Application

3-Indoleacetic acid (IAA) can be used as a building block to synthesize ,(±) harmacine using 4,4-diethoxybutan-1-amine via an acid-catalyzed acyl iminium ion cyclization reaction.
(±)-Harmacine is a vital step in the synthesis of a variety of indole alkaloids and dopamine/serotonin receptor ligands.[5] IAA can also be used in the preparation of alkaloid (±)-19-hydroxyibogamine.[6]

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves
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