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3469-07-6

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3469-07-6 Usage

General Description

5-Methoxy-1H-indene is a chemical compound with the molecular formula C10H10O. It is a derivative of indene, which is a bicyclic organic compound. The presence of a methoxy group in 5-position of the indene ring gives it unique properties and makes it useful for various applications in organic synthesis. It is a pale yellow colored solid and is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals. 5-Methoxy-1H-indene is also used in the production of fragrances and flavoring compounds due to its aromatic nature. Additionally, it has been studied for its potential medical applications, particularly in the treatment of neurological disorders. Moreover, it is used as a reagent in chemical reactions to introduce the indene moiety into organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 3469-07-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,6 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3469-07:
(6*3)+(5*4)+(4*6)+(3*9)+(2*0)+(1*7)=96
96 % 10 = 6
So 3469-07-6 is a valid CAS Registry Number.

3469-07-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Methoxy-1H-indene

1.2 Other means of identification

Product number -
Other names 1H-Indene,5-methoxy

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3469-07-6 SDS

3469-07-6Upstream product

3469-07-6Relevant articles and documents

AuCl3-Catalyzed Ring-Closing Carbonyl–Olefin Metathesis

Wang, Rui,Chen, Yi,Shu, Mao,Zhao, Wenwen,Tao, Maoling,Du, Chao,Fu, Xiaoya,Li, Ao,Lin, Zhihua

supporting information, p. 1941 - 1946 (2020/02/11)

Compared with the ripeness of olefin metathesis, exploration of the construction of carbon–carbon double bonds through the catalytic carbonyl–olefin metathesis reaction remains stagnant and has received scant attention. Herein, a highly efficient AuCl3-catalyzed intramolecular ring-closing carbonyl–olefin metathesis reaction is described. This method features easily accessible starting materials, simple operation, good functional-group tolerance and short reaction times, and provides the target cyclopentenes, polycycles, benzocarbocycles, and N-heterocycle derivatives in good to excellent yields.

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