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Benzenemethanol, 2-(acetyloxy)-4-methoxy-α-methylene-, acetate is a complex organic compound with the chemical formula C11H12O5. It is a derivative of benzyl alcohol, featuring a benzene ring with a hydroxyl group attached to the alpha carbon, which is further modified with an acetyloxy and methoxy group at the 2 and 4 positions, respectively. Benzenemethanol, 2-(acetyloxy)-4-methoxy-a-methylene-, acetate is also known as 2-(acetyloxy)-4-methoxy-α-methylenebenzyl acetate. It is a colorless liquid with a molecular weight of 224.21 g/mol. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain antibiotics and pesticides. Its chemical structure and reactivity make it a valuable building block in organic synthesis, allowing for the creation of a wide range of molecules with diverse applications.

78812-98-3

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78812-98-3 Usage

Chemical compound

Benzenemethanol, 2-(acetyloxy)-4-methoxy-α-methylene-, acetate

Classification

Ester derivative of salicylic acid

Use

Nonsteroidal anti-inflammatory drug (NSAID)

Properties

Analgesic, anti-inflammatory, antipyretic

Commonly used for

Pain relief, inflammation reduction, fever reduction

Medical conditions treated

Arthritis, headache, muscle aches

Caution

Should be used under the guidance of a healthcare professional

Potential side effects

May have interactions with other medications

Check Digit Verification of cas no

The CAS Registry Mumber 78812-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,1 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78812-98:
(7*7)+(6*8)+(5*8)+(4*1)+(3*2)+(2*9)+(1*8)=173
173 % 10 = 3
So 78812-98-3 is a valid CAS Registry Number.

78812-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-acetoxy-4-methoxyphenyl)vinyl acetate

1.2 Other means of identification

Product number -
Other names -

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:78812-98-3 SDS

78812-98-3Relevant academic research and scientific papers

Photolysis of Enol Acetates and α-Bromo Derivatives of o-(Acyloxy)acetophenones

Garcia, Hermenegildo,Martinez-Utrilla, Roberto,Miranda, Miguel A.

, p. 589 - 598 (2007/10/02)

UV irradiation of enol acetates 3a-g in benzene gives mainly o-(acetoxy)acetophenones 2 and 2-methylchromones 4. Under the same conditions, the dimethyl derivatives 3h and 3i remain unaffected.The α-bromo ketone 5a gives rise to mixtures of o-(acetoxy)acetophenone (2a), the diketone 6, and/or α-acetoxy-o-hydroxyacetophenone (7), depending on the irradiation conditions.The similarities and differences between the two series of experiments, as well as their possible mechanistic implications, are discussed.

PHOTOCYCLIZATION OF ENOL ACETATES OF o-ACETOXYACETOPHENONES TO CHROMONES

Garcia, Hermenegildo,Martinez-Utrilla, Roberto,Miranda, Miguel Angel

, p. 1749 - 1750 (2007/10/02)

Enol acetates of o-acetoxyacetophenones give chromones upon irradiation with uv-light.

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