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13336-31-7

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13336-31-7 Usage

Chemical Properties

white to light yellow crystal powder

Uses

4-Methoxy-1-indanone is suitable for use in the comparative study of the effect of different substituents on various benzo-fused ketones on the reaction kinetics by studying the biocatalysed oxidation reaction.It may be used in the following studies:Synthesis of isomeric mixture of oximes.As a starting material in the synthesis of benzo-fused indolizidine and 4-methoxy-1-indanyl compound.Synthesis of 4-methoxy-5-nitro-1-indanone by nitration reaction.As one of the reactant in the synthesis of E-2-chloro-8-methyl-3-[(4′-methoxy-1′-indanoyl)-2′-methyliden]-quinoline (IQ), a quinoline derivative.

General Description

4-Methoxy-1-indanone, a benzo-fused ketone is a 1-indanone derivative. Its synthesis has been reported.

Check Digit Verification of cas no

The CAS Registry Mumber 13336-31-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,3 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13336-31:
(7*1)+(6*3)+(5*3)+(4*3)+(3*6)+(2*3)+(1*1)=77
77 % 10 = 7
So 13336-31-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O2/c1-12-10-4-2-3-7-8(10)5-6-9(7)11/h2-4H,5-6H2,1H3

13336-31-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methoxy-1-indanone

1.2 Other means of identification

Product number -
Other names 4-methoxy-2,3-dihydroinden-1-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:13336-31-7 SDS

13336-31-7Relevant articles and documents

Kinetic resolution of racemic benzofused alcohols catalysed by HMFO variants in presence of natural deep eutectic solvents

Fraaije, Marco,Lon?ar, Nikola,de Gonzalo, Gonzalo

, (2022/03/01)

5-Hydroxymethylfurfural oxidase (HMFO) has demonstrated to be a useful biocatalyst for the selective oxidation of alcohols employing oxygen as mild oxidant with no requirement of expensive organic cofactors. This wild-type HMFO biocatalyst and an engineered thermostable variant have been tested in the kinetic resolution of different benzofused alcohols. The use of natural deep eutectic solvents was also explored in HMFO-catalysed oxidation of alcohols. The oxidation of racemic 1-indanol showed a higher conversion and selectivity in presence of 60% v/v of different NADES, especially for those containing carbohydrates. By choosing properly the biocatalyst and the NADES, good enantioselectivity values can be obtained, demonstrating the advantages of employing these neoteric solvents in biocatalysed processes.

Arylphosphine oxide and arylphosphine sulfide compounds, and preparation method and application thereof

-

Paragraph 0030; 0034-0037, (2019/06/07)

The invention discloses arylphosphine oxide and arylphosphine sulfide compounds, and a preparation method and an application thereof. The arylphosphine oxide and arylphosphine sulfide compounds can beused as an HIF-2alpha inhibitor to prepare drugs for treating and/or preventing diseases or symptoms related with an anoxic induction factor 2alpha in mammals. The structural formula of the arylphosphine oxide and arylphosphine sulfide compounds is shown in the description.

Synthesis and biological evaluation of pyridine-linked indanone derivatives: Potential agents for inflammatory bowel disease

Kadayat, Tara Man,Banskota, Suhrid,Bist, Ganesh,Gurung, Pallavi,Magar, Til Bahadur Thapa,Shrestha, Aarajana,Kim, Jung-Ae,Lee, Eung-Seok

, p. 2436 - 2441 (2018/06/18)

A series of pyridine-linked indanone derivatives were designed and synthesized to discover new small molecules for the treatment of inflammatory bowel disease (IBD). Compounds 5b and 5d exhibited strongest inhibitory activity against TNF-α-induced monocyte adhesion to colon epithelial cells (an in vitro model of colitis). In TNBS (2,4,6-trinitrobenzenesulfonic acid)-induced rat colitis model, oral administration of the compounds 5b and 5d ameliorated colitis with significant recovery in altered expressions of E-cadherin, TNF-α and IL-1β expressions, indicating 5b and 5d as potential agents for therapeutics development against IBD.

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