7-Nitroindole, 98%

Name: 7-Nitroindole, 98% | 6960-42-5
Brand: J&K Chemical
SKU: JK251892_25_G
Price: 863.4 USD
Availability: OutOfStock

Cat. No JK251892_25_G

Vendor: J&K Chemical

Product Information

Product Name

7-Nitroindole, 98%

Brand Name

J&K

Product Number

251892

CAS

6960-42-5

Molecular Formula

C8H6N2O2

Molecular Weight

162.15

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

23396

IUPAC Name

7-nitro-1H-indole

InChI Key

LZJGQIVWUKFTRD-UHFFFAOYSA-N

SMILES

C1=CC2=C(C(=C1)N+(=O)O-)NC=C2

Properties

Melting Point

94-98

Safety Information

Signal Word

Danger

Hazard Statement

H340

Precautionary Statement

P203

P280

P318

P405

P501

References Data Source From Pubchem

Enantioselective N-Alkylation of Nitroindoles under Phase-Transfer Catalysis

Publication Name: Synthesis

Publication Date: 2019-11-26

DOI: 10.1055/s-0039-1690751

Enzymgesteuerte Indigoproduktion

Publication Name: BIOspektrum

Publication Date: 2018-06-25

DOI: 10.1007/s12268-018-0938-1

Human Babesiosis: Pathogens, Prevalence, Diagnosis, and Treatment

Publication Name: Current Clinical Microbiology Reports

Publication Date: 2015-09-28

DOI: 10.1007/s40588-015-0025-z

Alkylation with Alkenes

Publication Name: Science of Synthesis

Publication Date: 2015

Synthesis of Quinoline-Based Anion Receptors and Preliminary Anion Binding Studies with Selected Derivatives

Publication Name: Synthesis

Publication Date: 2014-12-03

DOI: 10.1055/s-0034-1379605

7-Nitroindole, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Enantioselective N-Alkylation of Nitroindoles under Phase-Transfer Catalysis

Enzymgesteuerte Indigoproduktion

Human Babesiosis: Pathogens, Prevalence, Diagnosis, and Treatment

Alkylation with Alkenes

Synthesis of Quinoline-Based Anion Receptors and Preliminary Anion Binding Studies with Selected Derivatives

7-Nitroindole, 98%

6-Bromo-1H-indole-3-carbonitrile

Azepino[4,3-b]indole-2(1H)-carboxylic acid, 8-bromo-3,4,5,6-tetrahydro-, 1,1-dimethylethyl ester

6-Ethoxy-1H-indole

5-Ethylindole

trans-3-Indoleacrylic acid

rel-(3aR,7aS)-Octahydro-1H-isoindole

1-Methyl-2,3-dihydro-1H-isoindole hydrochloride

1-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

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7-Nitroindole, 98%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Enantioselective N-Alkylation of Nitroindoles under Phase-Transfer Catalysis

Enzymgesteuerte Indigoproduktion

Human Babesiosis: Pathogens, Prevalence, Diagnosis, and Treatment

Alkylation with Alkenes

Synthesis of Quinoline-Based Anion Receptors and Preliminary Anion Binding Studies with Selected Derivatives

7-Nitroindole, 98%

Related Product

6-Bromo-1H-indole-3-carbonitrile

Azepino[4,3-b]indole-2(1H)-carboxylic acid, 8-bromo-3,4,5,6-tetrahydro-, 1,1-dimethylethyl ester

6-Ethoxy-1H-indole

5-Ethylindole

trans-3-Indoleacrylic acid

rel-(3aR,7aS)-Octahydro-1H-isoindole

1-Methyl-2,3-dihydro-1H-isoindole hydrochloride

1-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole

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