634-20-8

Basic information

• Product Name: 2-Acetoxyphenylmethanediol diacetate
• Synonyms: (2-Acetoxyphenyl)methanediol diacetate;2-[Bis(acetyloxy)methyl]phenol acetate;2-Acetoxyphenylmethanediol diacetate;Acetylsalicylaldehyde diacetate;Salicylaldehyde triacetate;Toluene-α,α,2-triol triacetate
• CAS NO: 634-20-8
• Molecular Formula: C₁₃H₁₄O₆
• Molecular Weight: 266.2467
• Mol File: 634-20-8.mol
• Article Data: 38

Chemical Properties

• Boiling Point: 352.5°Cat760mmHg
• Flash Point: 154.1°C
• Appearance: /
• Density: 1.226g/cm³
• Vapor Pressure: 3.81E-05mmHg at 25°C
• Refractive Index: 1.506
• CAS DataBase Reference: 2-Acetoxyphenylmethanediol diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Acetoxyphenylmethanediol diacetate(634-20-8)
• EPA Substance Registry System: 2-Acetoxyphenylmethanediol diacetate(634-20-8)

Safety Data

• Hazardous Substances Data: 634-20-8(Hazardous Substances Data)

Usage

Physical Properties

Color: White
Form: Crystalline substance

Medical Uses

Pain reliever
Fever reducer
Anti-inflammatory medication
Blood thinner (to reduce the risk of heart attack and stroke)

Mechanism of Action

Inhibits the production of prostaglandins

Availability

Over-the-counter

Cautionary Notes

Should be used under the guidance of a healthcare professional
Potential side effects and interactions with other medications

InChI:InChI=1/C13H14O6/c1-8(14)17-12-7-5-4-6-11(12)13(18-9(2)15)19-10(3)16/h4-7,13H,1-3H3

Upstream product

• 252-72-2 6H,12H-6,12-epoxydibenzo[b,f][1,5]dioxocine 
• 108-24-7 acetic anhydride 
• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 5663-67-2 2-acetoxybenzaldehyde 
• 55230-18-7 2-(butyryloxy)benzaldehyde 
• 90-02-8 salicylaldehyde 
• 1118-68-9 dimethylaminoacetic acid 
• 7664-93-9 sulfuric acid 
• 7719-12-2 phosphorus trichloride 
• 89-95-2 2-methyl-benzyl alcohol 
• 533-18-6 2-methylphenyl acetate 
• 638-38-0 manganese(II) acetate 

Downstream Products

• 5663-67-2 2-acetoxybenzaldehyde 
• 108-24-7 acetic anhydride 
• 90-02-8 salicylaldehyde 
• 89-95-2 2-methyl-benzyl alcohol 
• 878-00-2 4-formylphenyl acetate 
• 140-11-4 Benzyl acetate 

Relevant articles and documents

REINVESTIGATION OF THE SYNTHETIC REACTION OF DIMETHYLAMINO-1,3-INDANDIONE.

One step preparation of dimethylamino-1,3-indandione (1) from salicyladehyde with glycine betaine was reinvestigated. Reaction conditions to give the best yield of 1, characterization of a minor product (2-acetoxybenzylidene diacetate), and reaction pathw

SiO2@FeSO4 nano composite as nanocatalyst for the green synthesis 1,1-diacetates from aldehydes under solvent-free conditions

Aldehydes compounds selective converted to 1,1-diacetates as protective reagent with SiO2@FeSO4 nano composite as effective nano catalyst at room temperature under solvent-free condition and acetic anhydride (Ac2O) as acet

Poly(4-vinylpyridinium) perchlorate as an efficient solid acid catalyst for the chemoselective preparation of 1,1-diacetates from aldehydes under solvent-free conditions

Poly(4-vinylpyridinium) perchlorate has been used as a supported, recyclable, environmentally-benign catalyst for the formation of acylals from aliphatic and aromatic aldehydes in good to excellent yields under solvent-free conditions. Notably, the reaction conditions were tolerant of ketones. This methodology offers several distinct advantages, including its operational simplicity and high product yield, as well as being green in terms of avoiding the use of toxic catalysts and solvents. Furthermore, the catalyst can be recovered and reused several times without any loss in its activity.