14216-34-3 Usage
Pharmaceutical intermediate
Used in the synthesis of various drugs 2-((methoxycarbonyl)oxy)benzoic acid serves as a key component in the production of different pharmaceutical compounds.
Anti-inflammatory properties
Offers relief from inflammation This chemical compound has the ability to reduce inflammation, making it a potentially useful ingredient in anti-inflammatory medications.
Industrial applications
Production of dyes, perfumes, and other products 2-((methoxycarbonyl)oxy)benzoic acid is not only limited to pharmaceutical use but also plays a role in the creation of dyes, perfumes, and other industrial items.
Physical appearance
White crystalline powder The compound has a solid, white, and crystalline form.
Solubility
Soluble in organic solvents like ethanol and acetone 2-((methoxycarbonyl)oxy)benzoic acid dissolves easily in specific organic solvents, which can be important for its applications and handling.
Stability
Relatively stable under normal conditions The compound does not react aggressively under typical circumstances, making it relatively safe to work with.
Reactivity
Violent reaction with strong oxidizing agents While generally stable, 2-((methoxycarbonyl)oxy)benzoic acid can cause fire and explosion hazards when it comes into contact with strong oxidizers.
Check Digit Verification of cas no
The CAS Registry Mumber 14216-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,1 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14216-34:
(7*1)+(6*4)+(5*2)+(4*1)+(3*6)+(2*3)+(1*4)=73
73 % 10 = 3
So 14216-34-3 is a valid CAS Registry Number.
14216-34-3Relevant academic research and scientific papers
8-Acyloxy-1,3-benzoxazine-2,4-diones as siderophore components for antibiotics
Wittmann,Scherlitz-Hofmann,Mollmann,Ankel-Fuchs,Heinisch
, p. 752 - 757 (2007/10/03)
8-Acyloxy-1,3-benzoxazine-2,4-diones as masked catechol derivatives represent a novel type of siderophore components, whose growth promoting activity is low or not existing if tested alone. But after conjugation with β-lactam antibiotics the resulting con
