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925441-35-6

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925441-35-6 Usage

General Description

2,6-Dimethyl-4-fluorobenzaldehyde is a chemical compound with the molecular formula C9H9FO. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. This chemical is also utilized in the manufacturing of fragrances and flavors. 2,6-Dimethyl-4-fluorobenzaldehyde has a distinctive aroma and is often used as a fragrance ingredient in various consumer products. It is important to handle this chemical with care as it may be toxic if ingested or inhaled, and can cause irritation to the skin and eyes upon contact.

Check Digit Verification of cas no

The CAS Registry Mumber 925441-35-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,5,4,4 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 925441-35:
(8*9)+(7*2)+(6*5)+(5*4)+(4*4)+(3*1)+(2*3)+(1*5)=166
166 % 10 = 6
So 925441-35-6 is a valid CAS Registry Number.

925441-35-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Fluoro-2,6-dimethylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 5-Fluoro-3-formyl-m-xylene

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:925441-35-6 SDS

925441-35-6Relevant articles and documents

Critical factors in determining the heterolytic versus homolytic bond cleavage of terminal oxidants by Iron(III) porphyrin complexes

Yokota, Sawako,Fujii, Hiroshi

, p. 5127 - 5137 (2018)

Heterolytic versus homolytic cleavage of the metal-bound terminal oxidant is the key for determining the nature of reactive intermediates in metalloenzymes and metal catalyzed oxygenation reactions. Here, we study the bond cleavage process of hypochlorite

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