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72482-15-6

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72482-15-6 Usage

General Description

3-Chloro-4-Methoxysalicylaldehyde is a chemical compound with the molecular formula C8H7ClO3. It is a white to light yellow solid that is soluble in organic solvents. 3-Chloro-4-Methoxysalicylaldehyde is commonly used as a reagent in organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. It is also used in the production of dyes and pigments. 3-Chloro-4-Methoxysalicylaldehyde has potential applications in the fields of medicine, agriculture, and materials science due to its versatile reactivity and unique properties. However, it should be handled with care due to its potential harmful effects if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 72482-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,8 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72482-15:
(7*7)+(6*2)+(5*4)+(4*8)+(3*2)+(2*1)+(1*5)=126
126 % 10 = 6
So 72482-15-6 is a valid CAS Registry Number.

72482-15-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-2-hydroxy-4-methoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-Chloro-4-methoxysalicylaldehyde

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:72482-15-6 SDS

72482-15-6Relevant articles and documents

TRICYCLIC INHIBITORS OF THE BCL6 BTB DOMAIN PROTEIN-PROTEIN INTERACTION AND USES THEREOF

-

Paragraph 00257, (2019/07/13)

The present application relates to compounds of Formula (I) or pharmaceutically acceptable salts, solvates and/or prodrugs thereof, to compositions comprising these compounds or pharmaceutically acceptable salts, solvates and/or prodrugs thereof, and various uses in the treatment of diseases, disorders or conditions that are treatable by inhibiting interactions with BCL6 BTB, such as cancer.

2,2,6,6-Tetramethylpiperidine-catalyzed, ortho-selective chlorination of phenols by sulfuryl chloride

Saper, Noam I.,Snider, Barry B.

, p. 809 - 813 (2014/04/03)

2,2,6,6-Tetramethylpiperidine (TMP)-catalyzed (1- 10%) chlorinations of phenols by SO2Cl2 in aromatic solvents are more ortho selective than with primary and less hindered secondary amine catalysts. Ortho-selective chlorination is successful even with electron deficient phenols such as 2-hydroxybenzaldehyde and 2'- hydroxyacetophenone. Notably, ortho selectivity increases with the reaction temperature. On the other hand, tetraalkylammonium chloride-catalyzed chlorinations are moderately para selective.

1,2-benzisoxazoloxyacetic acids and related compounds

-

, (2008/06/13)

Novel 1,2-benzisoxazoloxyacetic acids and related compounds, methods for preparing same and methods of treatment by administering compositions containing such a compound are described. These compounds are useful as diuretic, uricosuric and antihypertensive agents.

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