1-Iodo-2-naphthol, 97%

Name: 1-Iodo-2-naphthol, 97% | 2033-42-3
Brand: J&K Chemical
SKU: JK620114_5_G
Price: 131.23 USD
Availability: OutOfStock

Cat. No JK620114_5_G

Vendor: J&K Chemical

Product Information

Product Name

1-Iodo-2-naphthol, 97%

Brand Name

J&K

Product Number

620114

CAS

2033-42-3

Molecular Formula

C10H7IO

Molecular Weight

270.07

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

16250

IUPAC Name

1-iodonaphthalen-2-ol

InChI Key

JEVGGOSILOIIHN-UHFFFAOYSA-N

SMILES

C1=CC=C2C(=C1)C=CC(=C2I)O

Properties

Melting Point

92-96

Boiling Point

307

Safety Information

Storage Condition

Store at 2-8℃

References Data Source From Pubchem

Iodination of Arenes with Ammonium Salts and Iodine(III) Reagents

Publication Name: Science of Synthesis

Publication Date: 2025

Cascade Radical Cyclization to Vinylogous Carbonates/Carbamates for the Synthesis of Oxa- and Aza-Angular Triquinanes: Diastereoselectivity Depends on the Ring Size of Radical Precursor

Publication Name: Synthesis

Publication Date: 2018-07-11

DOI: 10.1055/s-0036-1589541

Metal-Mediated Reactions

Publication Name: Helicene Chemistry

Publication Date: 2016-11-05

DOI: 10.1007/978-3-662-53168-6_5

Catalytic Transformations of Alkynes via Ruthenium Vinylidene and Allenylidene Intermediates

Publication Name: Topics in Organometallic Chemistry

Publication Date: 2014

DOI: 10.1007/3418_2014_81

Ecofriendly Iodination of Activated Aromatics and Coumarins Using Potassium Iodide and Ammonium Peroxodisulfate

Publication Name: Synthesis

Publication Date: 2010-03-12

DOI: 10.1055/s-0029-1218698

1-Iodo-2-naphthol, 97%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Iodination of Arenes with Ammonium Salts and Iodine(III) Reagents

Cascade Radical Cyclization to Vinylogous Carbonates/Carbamates for the Synthesis of Oxa- and Aza-Angular Triquinanes: Diastereoselectivity Depends on the Ring Size of Radical Precursor

Metal-Mediated Reactions

Catalytic Transformations of Alkynes via Ruthenium Vinylidene and Allenylidene Intermediates

Ecofriendly Iodination of Activated Aromatics and Coumarins Using Potassium Iodide and Ammonium Peroxodisulfate