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2,6-DIMETHYL-4-FLUOROBENZALDEHYDE, with the molecular formula C9H9FO, is a chemical compound that serves as a crucial intermediate in the synthesis of various pharmaceuticals and agrochemicals. Characterized by its distinctive aroma, it is also widely used in the fragrance and flavor industry, adding a unique scent to a range of consumer products. Due to its potential toxicity and irritant properties, it is essential to handle this chemical with caution to avoid ingestion, inhalation, or skin and eye contact.

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  • 925441-35-6 Structure
  • Basic information

    1. Product Name: 2,6-DIMETHYL-4-FLUOROBENZALDEHYDE
    2. Synonyms: 2,6-DIMETHYL-4-FLUOROBENZALDEHYDE;5-Fluoro-3-formyl-m-xylene
    3. CAS NO:925441-35-6
    4. Molecular Formula: C9H9FO
    5. Molecular Weight: 152.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 925441-35-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 229.5±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.103±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,6-DIMETHYL-4-FLUOROBENZALDEHYDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,6-DIMETHYL-4-FLUOROBENZALDEHYDE(925441-35-6)
    11. EPA Substance Registry System: 2,6-DIMETHYL-4-FLUOROBENZALDEHYDE(925441-35-6)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 925441-35-6(Hazardous Substances Data)

925441-35-6 Usage

Uses

Used in Pharmaceutical Industry:
2,6-DIMETHYL-4-FLUOROBENZALDEHYDE is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medications. Its unique chemical structure allows it to be a key component in the production of therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2,6-DIMETHYL-4-FLUOROBENZALDEHYDE is utilized as an intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its role in these applications helps to improve agricultural productivity and crop protection.
Used in Fragrance Industry:
2,6-DIMETHYL-4-FLUOROBENZALDEHYDE is used as a fragrance ingredient in various consumer products, including perfumes, cosmetics, and personal care items. Its distinctive aroma adds a unique scent profile to these products, enhancing their appeal to consumers.
Used in Flavor Industry:
This chemical compound is also employed as a flavoring agent in the food and beverage industry. Its distinctive taste and aroma contribute to the flavor profiles of various products, providing a unique sensory experience for consumers.

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

COMPOUNDS, COMPOSITIONS AND METHODS FOR HISTONE LYSINE DEMETHYLASE INHIBITION

-

Paragraph 0737; 0789, (2022/03/09)

The present disclosure relates generally to compounds and pharmaceutical compositions for the selective inhibition of histone lysine demethylase5 (KDM5), particularly KDM5B, and methods of their use in treating conditions and diseases associated with KDM5 activity.

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