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76413-89-3

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76413-89-3 Usage

General Description

"2H-Inden-2-one, 1,3-dihydro-5-methoxy-" is a chemical compound with the molecular formula C10H10O2. 2H-INDEN-2-ONE, 1,3-DIHYDRO-5-METHOXY- has a wide range of applications in the chemical industry and has been widely used in theoretical research. Its structure consists of an indenone backbone, characterized by a fused cyclopentadiene and benzene ring, substituted by a methoxy group at the 5th position. This chemical is generally stored in a cool, dry place to ensure its stability and minimize reactivity. Its precise effects on human health and the environment are not well-studied, so caution should be taken while handling it.

Check Digit Verification of cas no

The CAS Registry Mumber 76413-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,1 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76413-89:
(7*7)+(6*6)+(5*4)+(4*1)+(3*3)+(2*8)+(1*9)=143
143 % 10 = 3
So 76413-89-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O2/c1-12-10-3-2-7-4-9(11)5-8(7)6-10/h2-3,6H,4-5H2,1H3

76413-89-3SDS

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-inden-2(3H)-one

1.2 Other means of identification

Product number -
Other names 5-methoxy-1,3-dihydroinden-2-one

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:76413-89-3 SDS

76413-89-3Relevant articles and documents

Facile transformation of benzocyclobutenones into 2,3-benzodiazepines via 4π-8π tandem electrocyclic reactions involving net insertion of diazomethylene compounds

Matsuya, Yuji,Ohsawa, Noriko,Nemoto, Hideo

, p. 13072 - 13073 (2008/02/08)

Efficient transformations of benzocyclobutenones into 2,3-benzodiazepines by a formal insertion of diazomethylene compounds are described. This sequential process includes nucleophilic addition of diazomethylene anion, oxy-anion accelerated o-quinodimethane formation by an electrocyclic ring-opening reaction, and 8π-electrocyclization in one-pot under remarkably mild conditions. Intermediary oxy-anion plays an important role for the efficient transformations. Copyright

Novel guanidinobenzamides

-

, (2008/06/13)

Compounds of formula IA and IB are new where the variables R1 through R10 have the values set forth herein. Such compounds have use in treating diseases such as obesity and type II diabetes, and may be provided as pharmaceutical form

Synthetic entry into yohimbinoid alkaloids and novel synthesis of (±)-17-methoxy-hexadehydroyohimbane

Pandit,Das,Chatterjee

, p. 4235 - 4239 (2007/10/02)

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