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1204298-54-3

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1204298-54-3 Usage

General Description

3,5-Dichloro-2,6-dihydroxybenzaldehyde is a chemical compound that is a derivative of benzaldehyde. It contains two chlorine atoms and two hydroxyl groups attached to a benzene ring. 3,5-Dichloro-2,6-dihydroxybenzaldehyde can be used in various chemical reactions and synthesis processes as a building block or intermediate. It is also used in the production of pharmaceuticals, agrochemicals, and other industrial applications. 3,5-Dichloro-2,6-dihydroxybenzaldehyde has potential uses in the development of new drugs and materials due to its structural properties and reactivity. Additionally, it may also be used in research and development as a reference compound for analytical purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 1204298-54-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,2,9 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1204298-54:
(9*1)+(8*2)+(7*0)+(6*4)+(5*2)+(4*9)+(3*8)+(2*5)+(1*4)=133
133 % 10 = 3
So 1204298-54-3 is a valid CAS Registry Number.

1204298-54-3SDS

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 3,5-Dichloro-2,6-dihydroxybenzaldehyde

1.2 Other means of identification

Product number -
Other names -

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:1204298-54-3 SDS

1204298-54-3Downstream Products

1204298-54-3Relevant articles and documents

A designed protein binding-pocket to control excited-state intramolecular proton transfer fluorescence

Lampkin, Bryan J.,Monteiro, Cecilia,Powers, Evan T.,Bouc, Paige M.,Kelly, Jeffery W.,Vanveller, Brett

, p. 1076 - 1080 (2019)

Excited-state intramolecular proton transfer involves a photochemical isomerization and creates the opportunity for the emission of two distinct wavelengths of light from a single fluorophore. The selectivity between these two wavelengths of emission is d

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