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5-Chlorovanillyl alcohol, a chemical compound with the formula C8H9ClO2, is a white to off-white crystalline solid. It is primarily recognized for its role as a precursor in the pharmaceutical industry for the synthesis of vanilloid compounds, which have been studied for their potential therapeutic applications in treating pain and inflammation. Due to its structural similarity to naturally occurring vanilloids, which exhibit biological activity, 5-chlorovanillyl alcohol is also a promising candidate for the development of new drugs. Furthermore, it finds use as a flavoring agent in the food industry and as a fragrance in the cosmetic industry, highlighting its versatility across different sectors.

20624-92-4

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20624-92-4 Usage

Uses

Used in Pharmaceutical Industry:
5-Chlorovanillyl alcohol is used as a precursor for the synthesis of vanilloid compounds for their potential therapeutic applications in treating various conditions, including pain and inflammation. Its structural similarity to naturally occurring vanilloids, which are known for their biological activity, makes it a promising candidate for the development of new drugs.
Used in Food Industry:
5-Chlorovanillyl alcohol is used as a flavoring agent, contributing to the taste profiles of various food products by imparting a characteristic flavor note.
Used in Cosmetic Industry:
In the cosmetic industry, 5-chlorovanillyl alcohol serves as a fragrance, enhancing the sensory experience of cosmetic products through its distinct aromatic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 20624-92-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,2 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20624-92:
(7*2)+(6*0)+(5*6)+(4*2)+(3*4)+(2*9)+(1*2)=84
84 % 10 = 4
So 20624-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H9ClO3/c1-12-7-3-5(4-10)2-6(9)8(7)11/h2-3,10-11H,4H2,1H3

20624-92-4 Well-known Company Product Price

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  • Alfa Aesar

  • (B25108)  3-Chloro-4-hydroxy-5-methoxybenzyl alcohol, 98%   

  • 20624-92-4

  • 1g

  • 126.0CNY

  • Detail
  • Alfa Aesar

  • (B25108)  3-Chloro-4-hydroxy-5-methoxybenzyl alcohol, 98%   

  • 20624-92-4

  • 5g

  • 416.0CNY

  • Detail
  • Alfa Aesar

  • (B25108)  3-Chloro-4-hydroxy-5-methoxybenzyl alcohol, 98%   

  • 20624-92-4

  • 25g

  • 1609.0CNY

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20624-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-(hydroxymethyl)-6-methoxyphenol

1.2 Other means of identification

Product number -
Other names 5-Chlorovanillyl alcohol

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:20624-92-4 SDS

20624-92-4Relevant academic research and scientific papers

Electrophilicity and nucleophilicity of commonly used aldehydes

Pratihar, Sanjay

, p. 5781 - 5788 (2014/07/22)

The present approach for determining the electrophilicity (E) and nucleophilicity (N) of aldehydes includes a kinetic study of KMNO4 oxidation and NaBH4 reduction of aldehydes. A transition state analysis of the KMNO4 promoted aldehyde oxidation reaction has been performed, which shows a very good correlation with experimental results. The validity of the experimental method has been tested using the experimental activation parameters of the two reactions. The utility of the present approach is further demonstrated by the theoretical versus experimental relationship, which provides easy access to E and N values for various aldehydes and offers an at-a-glance assessment of the chemical reactivity of aldehydes in various reactions. the Partner Organisations 2014.

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