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616195-96-1

2,6-dichloro-4-(hydroxyMethyl)benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

616195-96-1

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616195-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 616195-96-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,6,1,9 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 616195-96:
(8*6)+(7*1)+(6*6)+(5*1)+(4*9)+(3*5)+(2*9)+(1*6)=171
171 % 10 = 1
So 616195-96-1 is a valid CAS Registry Number.

616195-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dichloro-4-(hydroxymethyl)benzaldehyde

1.2 Other means of identification

Product number -
Other names 2,6-Dichloro-4-hydroxymethylbenzaldehyde

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:616195-96-1 SDS

616195-96-1Relevant articles and documents

THYROMIMETICS

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, (2022/01/05)

Compounds provided herein function as thyromimetics and have utility for treating diseases such as neurodegenerative disorders and fibrotic diseases. Pharmaceutical compositions containing such compounds are also provided, as are methods of their preparation.

NOVEL IMIDAZOLE DERIVATIVES AND THEIR USE AS PHARMACEUTICAL AGENTS

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Page/Page column 25, (2008/06/13)

Compounds of the general formula (I) are valuable therapeutics for the treatment of cancer and cancer related diseases.

Simple, short and efficient procedure for the preparation of hydroxyl- and hydroxymethyl-substituted 2,6-dichlorobenzaldehydes

Von Hirschheydt, Thomas,Voss, Edgar

, p. 2062 - 2065 (2007/10/03)

Hydroxyl- and hydroxymethyl-substituted 2,6-dichlorobenzaldehydes 1-4 have been obtained by lithiation of the corresponding TIPS-protected dichlorophenols or dichlorobenzylic alcohols followed by reaction with DMF and subsequent deprotection of the hydroxy group. Yields are high and formation of regioisomers is not observed.

2-(2,6-dichlorophenyl)-diarylimidazoles

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Page/Page column 7, (2010/11/29)

The invention is directed to compounds of formula (I), which are valuable therapeutics for the treatment of cancer and related diseases.

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