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24006-92-6

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24006-92-6 Usage

General Description

4,5-Dichloro-1,2-benzenedimethanol is a chemical compound with the molecular formula C8H8Cl2O2. It is a white crystalline solid that is used in the production of pharmaceuticals, agrochemicals, and other organic compounds. It has antimicrobial properties and is often used as a preservative in cosmetic and personal care products. The compound is synthesized through the chlorination of 1,2-benzenedimethanol, resulting in the substitution of chlorine atoms at the 4 and 5 positions on the benzene ring. 4,5-Dichloro-1,2-benzenedimethanol is considered to be moderately toxic and should be handled with care and in accordance with safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 24006-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,0 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24006-92:
(7*2)+(6*4)+(5*0)+(4*0)+(3*6)+(2*9)+(1*2)=76
76 % 10 = 6
So 24006-92-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H8Cl2O2/c9-7-1-5(3-11)6(4-12)2-8(7)10/h1-2,11-12H,3-4H2

24006-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-Dichloro-1,2-benzenedimethanol

1.2 Other means of identification

Product number -
Other names [4,5-dichloro-2-(hydroxymethyl)phenyl]methanol

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:24006-92-6 SDS

24006-92-6Relevant articles and documents

2,3-Dihalo- and 2,3,6,7-Tetrahaloanthracenes by Vollhardt Trimerization

Hoffmann, Hendrik,Mukanov, Diana,Ganschow, Michael,Rominger, Frank,Freudenberg, Jan,Bunz, Uwe H. F.

, p. 9826 - 9834 (2019/08/20)

We efficiently synthesized otherwise difficult to obtain 2,3- and 2,3,6,7-halogenated anthracenes with diverse east/west substituents. Key steps involve the (i) Vollhardt cyclization of bis(propargyl)benzenes with bis(trimethylsilyl)acetylene, (ii) halo-desilylation introducing chlorine, bromine, or iodine substituents, and (iii) dehydrogenation. Pd catalysis allows selective functionalization at the anthracenes' east/west positions. A tetrahydropentacene is synthesized and derivatized via the same strategy, employing tetrapropargylbenzene.

ALPHA-CINNAMIDE COMPOUNDS AND COMPOSITIONS AS HDAC8 INHIBITORS

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Paragraph 0930; 0931, (2016/10/04)

The present invention relates to inhibitors of histone deacetylases, in particular HDAC8, that are useful for the treatment of cancer and other diseases and disorders, as well as the synthesis and applications of said inhibitors.

GLUCOSYLCERAMIDE SYNTHASE INHIBITORS FOR THE TREATMENT OF DISEASES

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Paragraph 000286, (2015/04/15)

Described herein are compounds of Formula I, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or conditions associated with the enzyme glucosylceramide synthase (GCS).

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