14754-47-3 Usage
Uses
Used in Polymer Production:
Isocyanatosulfuric acid, 4-methoxyphenyl ester is used as a monomer or a precursor in the production of polymers for its ability to form stable and versatile polymeric materials.
Used in Adhesives:
In the adhesives industry, Isocyanatosulfuric acid, 4-methoxyphenyl ester is used as a component to enhance the bonding properties of adhesives, providing strong and durable adhesion.
Used in Coatings:
Isocyanatosulfuric acid, 4-methoxyphenyl ester is used in the formulation of coatings to improve their durability, resistance to environmental factors, and overall performance.
Used as a Reagent in Organic Synthesis:
In the field of organic synthesis, Isocyanatosulfuric acid, 4-methoxyphenyl ester serves as a reagent to facilitate various chemical reactions, contributing to the synthesis of complex organic compounds.
Used in Pharmaceutical Manufacturing:
Isocyanatosulfuric acid, 4-methoxyphenyl ester is utilized in the manufacturing of pharmaceuticals, where it may play a role in the synthesis of active pharmaceutical ingredients or as a component of drug formulations.
It is crucial to handle Isocyanatosulfuric acid, 4-methoxyphenyl ester with care due to its potential hazards to health and the environment if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 14754-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,5 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14754-47:
(7*1)+(6*4)+(5*7)+(4*5)+(3*4)+(2*4)+(1*7)=113
113 % 10 = 3
So 14754-47-3 is a valid CAS Registry Number.
14754-47-3Relevant academic research and scientific papers
Preparation and antimicrobial studies of acyclic sulfamates.
Gautun,Bergan,Carlsen
, p. 446 - 452 (2007/10/03)
A series of acyclic sulfamates have been prepared and tested for antimicrobial activity. Thus, the oxysulfonyl isocyanates, ROSO2NCO (1a, R = 4-methoxyphenyl; 1b, R = phenyl; 1c, R = 4-chlorophenyl and 1d, R = 2,2,2-trifluoroethyl) have been prepared in 76-91% yield from chlorosulfonyl isocyanate. Treatment of 1a-d with glycidol gave the glycidyl carbamates 2a d. Internal cyclisation afforded the corresponding 4-hydroxymethyl-2-oxazolidinones 3a-d, which in turn were hydrolysed to give the free amino alcohols 4a-d. The yields were in the range 39-85%. A preliminary agar diffusion test of 2a-d, 3a-d, 4a-d indicated 2a-d and 3c to be possible antimicrobial agents. A more thorough analysis of these compounds revealed a minimum inhibition concentration (MIC) of 128 and 64 mg l-1 for glycidyl p-methoxyphenoxysulfonylcarbamate (2a) and glycidyl phenoxysulfonylcarbamate (2b) respectively, against Branhamella catarrhalis.
