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4-(9H-fluoren-2-yl)butanoic acid is a chemical compound with the molecular formula C16H16O2. It is a white crystalline solid that is soluble in organic solvents. 4-(9H-fluoren-2-yl)butanoic acid is a derivative of butanoic acid, featuring a fluorenyl group attached to the 4-position of the butanoic acid backbone. The fluorenyl group, which is a part of the larger fluorene molecule, contributes to the compound's stability and reactivity. 4-(9H-fluoren-2-yl)butanoic acid is used in various applications, including the synthesis of pharmaceuticals and other organic compounds, due to its unique structural properties and potential to form stable intermediates in chemical reactions.

7250-03-5

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7250-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7250-03-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7250-03:
(6*7)+(5*2)+(4*5)+(3*0)+(2*0)+(1*3)=75
75 % 10 = 5
So 7250-03-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H16O2/c18-17(19)7-3-4-12-8-9-16-14(10-12)11-13-5-1-2-6-15(13)16/h1-2,5-6,8-10H,3-4,7,11H2,(H,18,19)

7250-03-5SDS

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-(9H-fluoren-2-yl)butanoic acid

1.2 Other means of identification

Product number -
Other names 4-Fluoren-2-yl-buttersaeure

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:7250-03-5 SDS

7250-03-5Relevant academic research and scientific papers

A convenient procedure for the synthesis of 1-tetralone dertivatives using a Suzuki coupling-Friedel-Crafts acylation sequence

Esteban, Gemma,Lopez-Sanchez, Miguel A.,Martinez, Ma. Eugenia,Plumet, Joaquin

, p. 197 - 212 (2007/10/03)

The reported 1-tetralone derivatives have been synthesized from arylbromides using as keys steps a Suzuki coupling followed by intramolecular Friedel-Crafts acylation.

Synthesis of Diazofluorene based Reagents as Photoactivatable Membrane Probes

Lala, Anil K.,Dixit, Rajiv R.

, p. 636 - 638 (2007/10/02)

We report the synthesis of diazofluorene based photoactivatable reagents, as analogues of fatty acids and alcohols for their use as probes for studying a membrane hydrophobic core.

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