7-Methoxy-2-tetralone, 95%

Name: 7-Methoxy-2-tetralone, 95% | 4133-34-0
Brand: J&K Chemical
SKU: JK126184_1_G
Price: 38.8 USD
Availability: OutOfStock

Cat. No JK126184_1_G

Vendor: J&K Chemical

Product Information

Product Name

7-Methoxy-2-tetralone, 95%

Brand Name

J&K

Product Number

126184

CAS

4133-34-0

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

77785

IUPAC Name

7-methoxy-3,4-dihydro-1H-naphthalen-2-one

InChI Key

XEAPZXNZOJGVCZ-UHFFFAOYSA-N

SMILES

COC1=CC2=C(CCC(=O)C2)C=C1

Safety Information

Storage Condition

Store at 2-8℃

References Data Source From Pubchem

A guide for asymmetric synthesis of morphine alkaloids

Publication Name: Medicinal Chemistry Research

Publication Date: 2024-11-21

DOI: 10.1007/s00044-024-03350-9

Fukuyama reduction, Fukuyama coupling and Fukuyama–Mitsunobu alkylation: recent developments and synthetic applications

Publication Name: Molecular Diversity

Publication Date: 2021-02-11

DOI: 10.1007/s11030-021-10194-7

Photocatalytic Oxidative C—C Bond Formation via Arene Radical Cation Intermediates

Publication Name: Science of Synthesis

Publication Date: 2018

Copper-Catalyzed Cleavage of Unstrained C–C Bonds for the Synthesis of 1-Acyloxy-2,2,6,6-tetramethylpiperidines from Cyclic or Acyclic Ketones

Publication Name: Synlett

Publication Date: 2017-07-13

DOI: 10.1055/s-0036-1590805

Alectinib

Publication Name: Pharmaceutical Substances

Publication Date: 2016

7-Methoxy-2-tetralone, 95%

Product Information

General Information

Safety Information

References Data Source From Pubchem

A guide for asymmetric synthesis of morphine alkaloids

Fukuyama reduction, Fukuyama coupling and Fukuyama–Mitsunobu alkylation: recent developments and synthetic applications

Photocatalytic Oxidative C—C Bond Formation via Arene Radical Cation Intermediates

Copper-Catalyzed Cleavage of Unstrained C–C Bonds for the Synthesis of 1-Acyloxy-2,2,6,6-tetramethylpiperidines from Cyclic or Acyclic Ketones

Alectinib