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114915-75-2

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114915-75-2 Usage

General Description

2-(1-oxo-1H-inden-2(3H)-ylidene)acetic acid is a chemical compound with a molecular formula C11H8O3. It is a derivative of indene, a bicyclic aromatic hydrocarbon, and it contains a carboxylic acid functional group and an inden-2(3H)-ylidene moiety. The compound may have potential applications in organic synthesis or medicinal chemistry, and its properties and reactivity are of interest to researchers. It is important to handle and store this chemical with proper precautions, as its exact hazards and risks are not available without specific information on its formulation and purity.

Check Digit Verification of cas no

The CAS Registry Mumber 114915-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,9,1 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114915-75:
(8*1)+(7*1)+(6*4)+(5*9)+(4*1)+(3*5)+(2*7)+(1*5)=122
122 % 10 = 2
So 114915-75-2 is a valid CAS Registry Number.

114915-75-2SDS

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 2-(3-oxo-1H-inden-2-ylidene)acetic acid

1.2 Other means of identification

Product number -
Other names indanylideneacetic acid

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:114915-75-2 SDS

114915-75-2Relevant articles and documents

Synthesis of the pentacylic core of (+)-salvileucalin B

Taber, Douglass F.,Paquette, Craig M.

, p. 3410 - 3413 (2014)

A concise preparation of the prochiral pentacyclic core of (+)-salvileucalin B is presented. The key feature in the synthesis is the Cu-catalyzed intramolecular cyclopropanation of a symmetrical indane-derived α-diazo β-keto ester. This symmetry is carrie

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