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5-Chloro-2-Hydroxy-4-Methylbenzaldehyde (5-Chloro-4-Methylsalicylaldehyde) is a chemical compound with the molecular formula C8H7ClO2 and a molar mass of 170.59 g/mol. It features a chlorine atom attached to a benzene ring, which also contains a hydroxy group and a methyl group, with an aldehyde functional group at an adjacent position on the ring. 5-Chloro-2-Hyroxy-4-Methylbenzaldehyde (5-Chloro-4-Methylsalicylaldehyde) is typically found as a light beige/yellowish solid and is recognized for its suitability for further chemical processing. Due to its potential to cause skin and eye irritation, caution is advised during handling, and it should be stored in a cool, well-ventilated area, away from oxidative agents.

3328-68-5

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3328-68-5 Usage

Uses

Used in Organic Synthesis:
5-Chloro-2-Hydroxy-4-Methylbenzaldehyde (5-Chloro-4-Methylsalicylaldehyde) is used as a key intermediate in the synthesis of various organic compounds. Its unique structure, which includes a chlorine atom, hydroxy group, and aldehyde functional group, makes it a versatile building block for the creation of a wide range of chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Chloro-2-Hydroxy-4-Methylbenzaldehyde (5-Chloro-4-Methylsalicylaldehyde) is used as a starting material for the development of new drugs. Its chemical properties allow for the formation of diverse molecular structures, which can be further modified to create potential therapeutic agents.
Used in Agrochemical Industry:
5-Chloro-2-Hydroxy-4-Methylbenzaldehyde (5-Chloro-4-Methylsalicylaldehyde) is also utilized in the agrochemical industry for the synthesis of various agrochemical products, such as pesticides and herbicides. Its reactivity and functional groups enable the creation of compounds with specific target effects on pests and weeds.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 5-Chloro-2-Hydroxy-4-Methylbenzaldehyde (5-Chloro-4-Methylsalicylaldehyde) is employed as a precursor for the production of dyes and pigments. Its chemical structure can be manipulated to yield a range of colors and properties, making it a valuable component in the formulation of various colorants.
Used in Flavor and Fragrance Industry:
5-Chloro-2-Hydroxy-4-Methylbenzaldehyde (5-Chloro-4-Methylsalicylaldehyde) is used as a raw material in the flavor and fragrance industry to create unique scents and flavors. Its aromatic properties allow for the development of novel fragrances and flavorings, contributing to the diversity of products in this sector.

Check Digit Verification of cas no

The CAS Registry Mumber 3328-68-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3328-68:
(6*3)+(5*3)+(4*2)+(3*8)+(2*6)+(1*8)=85
85 % 10 = 5
So 3328-68-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClO2/c1-5-2-8(11)6(4-10)3-7(5)9/h2-4,11H,1H3

3328-68-5SDS

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 5-chloro-2-hydroxy-4-methylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 5-chloro-4-methylsalicylaldehyde

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:3328-68-5 SDS

3328-68-5Relevant academic research and scientific papers

Pd-Catalyzed Ortho C-H Hydroxylation of Benzaldehydes Using a Transient Directing Group

Chen, Xiao-Yang,Ozturk, Seyma,Sorensen, Erik J.

supporting information, p. 6280 - 6283 (2017/12/08)

The direct Pd-catalyzed ortho C-H hydroxylation of benzaldehydes was achieved using 4-chloroanthranilic acid as the transient directing group, 1-fluoro-2,4,6-trimethylpyridnium triflate as the bystanding oxidant, and p-toluenesulfonic acid as the putative oxygen nucleophile. The unusual C-H chlorination and polyfluoroalkoxylation reactions signaled the importance of external nucleophiles to the outcome of Pd(IV) reductive eliminations.

Palladium(0)-catalyzed intramolecular heck reaction: A resourceful route for the synthesis of naphthoxepine naphthoxocine derivatives

Majumdar,Ansary, Inul,Sinha, Biswajit,Chattopadhyay, Buddhadeb

experimental part, p. 3593 - 3602 (2010/03/03)

The synthesis of oxocines and oxepines is difficult. Two efficient protocols have been developed for the construction of naphthoxepine and naphthoxocine derivatives by sequential Wittig olefination and intramolecular Heck reaction. Georg Thieme Verlag Stuttgart.

BENZOPYRAN COMPOUNDS USEFUL FOR TREATING INFLAMMATORY CONDITIONS

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Page 305, (2010/02/08)

The subject invention concerns methods and compounds that have utility in the treatment of a condition associated with cyclooxygenase-2 mediated disorders. Compounds of particular interest are benzopyrans and their analogs defined by formula (1). Wherein Z, X, R1, R2, R3, and R4 are as described in specification.

CHROMENE DERIVATIVES AS ANTI-INFLAMMATORY AGENTS

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Page 305, (2010/02/08)

The subject invention concerns methods and compounds that have utility in the treatment of a condition associated with cyclooxygenase-2 mediated disorders. Compounds of particular interest are benzopyrans and their analogs defined by formula (I). Wherein Z, X, R1, R2, R3, and R4 are as described in the specification.

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