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4-Nitrophenylcarbamyl fluoride, also known as 4-NPA or 4-nitrophenyl N-fluorocarboximide, is a chemical compound with the molecular formula C7H4FN2O4. It is a yellow crystalline solid that is soluble in water and polar organic solvents. 4-nitrophenylcarbamyl fluoride is primarily used as a reagent in the determination of cholinesterase activity, an enzyme that plays a crucial role in the nervous system. 4-Nitrophenylcarbamyl fluoride is a substrate for cholinesterases, and upon hydrolysis by the enzyme, it releases 4-nitrophenol, which can be easily quantified colorimetrically. This property makes it a valuable tool in the study of enzyme kinetics and the development of new drugs targeting cholinesterase. Additionally, it has been used in the synthesis of various pharmaceuticals and agrochemicals. Due to its reactivity and potential toxicity, it is important to handle 4-nitrophenylcarbamyl fluoride with care, following appropriate safety protocols.

351-92-8

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351-92-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 351-92-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 351-92:
(5*3)+(4*5)+(3*1)+(2*9)+(1*2)=58
58 % 10 = 8
So 351-92-8 is a valid CAS Registry Number.

351-92-8Relevant academic research and scientific papers

Syntheses of isocyanates via amines and carbonyl fluoride

Quan, Hengdao,Zhang, Ni,Zhou, Xiaomeng,Qian, Hua,Sekiya, Akira

, p. 26 - 30 (2015)

Isocyanates are widely used in many different areas, but the most common synthesis route-phosgene route cannot fit the more and more rigorous restriction of safety and environment. Here, a facile synthesis method of isocyanates via amines and carbonyl fluoride is proven feasibly by expanding its applications to the syntheses of nine different isocyanates. And two differences with the phosgene route are proposed. The reaction could occur under milder conditions and afford isocyanates in good yields, especially for the isocyanates containing electron withdrawing groups. It is appealing for industrial application.

Method for preparing isocyanate by using amine and carbonyl fluoride

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Paragraph 0065-0066, (2017/07/07)

The invention discloses an efficient synthesis method for preparing corresponding isocyanate by enabling carbonyl fluoride to directly react with amine. The efficient synthesis method mainly comprises the following two steps: carrying out acylation reaction on the amine and the carbonyl fluoride according to a preferable proportion in an anhydrous inertial organic solvent under a sealed environment and a proper reaction condition, thus generating an intermediate-carbamyl fluoride; (2) carrying out dehydrofluorination on the intermediate-carbamyl fluoride under normal pressure and the proper reaction condition, thus obtaining the target isocyanate. During a reaction process, addition of a catalyst is not needed, the reaction conditions are mild, excessive carbonyl fluoride and a used solvent during the reaction process can be efficiently recycled and reused, and a by-product HF can be commercially sold after being collected and refined.

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