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Methanediol, (3-fluorophenyl)-, diacetate, also known as 3-fluorophenyl methanediol diacetate, is an organic compound with the chemical formula C10H11FO4. It is a colorless to pale yellow liquid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound consists of a methanediol core with a 3-fluorophenyl group attached to one of the hydroxyl groups and two acetate groups esterified to the remaining hydroxyl groups. It is soluble in organic solvents and has a molecular weight of 214.19 g/mol. Due to its reactivity and potential applications in the synthesis of various compounds, it is an important chemical in the field of organic chemistry.

1479-26-1

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1479-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1479-26-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1479-26:
(6*1)+(5*4)+(4*7)+(3*9)+(2*2)+(1*6)=91
91 % 10 = 1
So 1479-26-1 is a valid CAS Registry Number.

1479-26-1SDS

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 3-fluorobenzaldehyde-1,1-diacetate

1.2 Other means of identification

Product number -
Other names 3-Fluor-benzaldiacetat

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:1479-26-1 SDS

1479-26-1Relevant academic research and scientific papers

Simple synthesis of geminal diacetates (Acylals) of aromatic aldehydes

Rahman, Motiur A. F. M.,Jahng, Yurngdong

, p. 1213 - 1220 (2006)

The geminal diacetates of aromatic aldehydes were prepared from corresponding aldehydes by refluxing with acetic anhydride without any catalysts or even any additional solvent. Copyright Taylor & Francis Group, LLC.

Preparation of geminal diacylates (acylals) of aldehydes - Scope and reactivity of aldehydes with acid anhydrides

Rahman, Motiur A. F. M.,Jahng, Yurngdong

, p. 379 - 383 (2007)

The geminal diacylates of a variety of aldehydes were prepared in good yields without any catalysts or solvent by simply refluxing the aldehydes with aliphatic acid anhydrides. The scope of the reactions and relative reactivities of aldehydes and acid anhydrides were examined. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

H3PW12O40-catalysed alkylation of arenes and diveratrylmethanes: Convenient routes to triarylmethanes and to symmetrical and unsymmetrical 9,10-diaryl-2,3,6,7-tetramethoxyanthracenes

Mohammadpoor-Baltork, Iraj,Moghadam, Majid,Tangestaninejad, Shahram,Mirkhani, Valiollah,Mohammadiannejad-Abbasabadi, Kazem,Khavasi, Hamid R.

scheme or table, p. 1357 - 1366 (2011/04/17)

An efficient method for the synthesis of triarylmethanes and difurylarylmethanes through solventless reactions between aldehydes and arenes in the presence of H3PW12O40 as a reusable catalyst under thermal and microwave irradiation conditions has been developed. H3PW12O40-catalysed one-pot consecutive Friedel-Crafts reactions between veratrole and aldehydes were also applied as a convenient protocol for the preparation of symmetrical 9,10-diaryl-2,3,6,7- tetramethoxyanthracenes.

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