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2,4-Dihydroxybenzil, also known as benzil, is a crystalline solid with the molecular formula C14H12O4. It is a dihydroxybenzene derivative characterized by the presence of two hydroxyl groups in its structure. This versatile chemical compound is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its antioxidant properties and potential applications in medicine and skin care make it a valuable compound in various industries.

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  • 87538-42-9 Structure
  • Basic information

    1. Product Name: 2,4-DIHYDROXYBENZIL
    2. Synonyms: 2,4-DIHYDROXYBENZIL
    3. CAS NO:87538-42-9
    4. Molecular Formula: C14H10O4
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 87538-42-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,4-DIHYDROXYBENZIL(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-DIHYDROXYBENZIL(87538-42-9)
    11. EPA Substance Registry System: 2,4-DIHYDROXYBENZIL(87538-42-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 87538-42-9(Hazardous Substances Data)

87538-42-9 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2,4-Dihydroxybenzil is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the development of new compounds with therapeutic and pesticidal properties.
Used in Dye Production:
2,4-Dihydroxybenzil is used as a key component in the production of dyes. Its chemical properties enable the creation of a wide range of colors, making it a valuable asset in the dye industry.
Used in Polymer Synthesis:
2,4-Dihydroxybenzil is utilized in the synthesis of polymers due to its reactive hydroxyl groups. These polymers find applications in various fields, including plastics, coatings, and adhesives.
Used as a Reagent in Organic Synthesis:
2,4-Dihydroxybenzil serves as a reagent in organic synthesis, facilitating various chemical reactions. Its presence can enhance the efficiency and selectivity of these reactions, making it an essential component in many organic synthesis processes.
Used in Medicine:
2,4-Dihydroxybenzil's antioxidant properties make it a potential candidate for use in medicine. Its ability to neutralize harmful free radicals can contribute to the development of treatments for various diseases and conditions.
Used in Skin Care:
The antioxidant properties of 2,4-dihydroxybenzil also make it a promising ingredient in skin care products. Its potential to protect the skin from oxidative stress and promote overall skin health can be beneficial in the development of skincare formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 87538-42-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,3 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87538-42:
(7*8)+(6*7)+(5*5)+(4*3)+(3*8)+(2*4)+(1*2)=169
169 % 10 = 9
So 87538-42-9 is a valid CAS Registry Number.

87538-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,4-dihydroxyphenyl)-2-phenylethane-1,2-dione

1.2 Other means of identification

Product number -
Other names 2,4-Dihydroxy-benzil

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:87538-42-9 SDS

87538-42-9Relevant articles and documents

Iron-catalyzed ortho-selective functionalization of phenols: A straightforward strategy towards the 2′-hydroxyphenyl-1,2-dione skeleton

Guo, Xingwei,Li, Wenjuan,Li, Zhiping

experimental part, p. 5787 - 5790 (2011/01/04)

An iron-catalyzed ortho-functionalization of phenols was developed. The reactions of simple phenols with α-hydroxy ketones provide a novel and efficient method to construct 2′-hydroxyphenyl-1,2-dione derivatives. An iron-catalyzed ortho-functionalization of phenols was developed. The reactions of simple phenols with α-hydroxy ketonesprovide a novel and efficient method to construct 2′-hydroxyphenyl-1,2-dione derivatives.

FACILE OXIDATION OF o-HYDROXYPHENYL BENZYL KETONES TO UNSYMMETRICAL BENZILS WITH DIMETHYL SULPHOXIDE/POTASSIUM HYDROXIDE

Saxena, Shabnam,Jain, P. K.,Makrandi, J. K.,Grover, S. K.

, p. 3401 - 3402 (2007/10/02)

o-Hydroxyphenyl benzyl ketones on treatment with dimethyl sulphoxide and powdered potassium hydroxide have been found to undergo facile oxidation to the corresponding benzils.

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