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Diphenyl-carbamic acid-(4-nitro-phenyl ester) is a chemical compound with the molecular formula C19H14N2O5. It is an ester derivative of diphenylcarbamic acid, where one of the phenyl rings is substituted with a nitro group. diphenyl-carbamic acid-(4-nitro-phenyl ester) is characterized by its yellow crystalline appearance and is soluble in organic solvents such as ethanol and ether. It is primarily used in the synthesis of pharmaceuticals and agrochemicals due to its reactivity and structural properties. The compound's chemical structure features a carbamic acid group esterified with a 4-nitrophenyl group, which contributes to its potential applications in the development of active ingredients for various chemical industries.

3848-46-2

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3848-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3848-46-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,4 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3848-46:
(6*3)+(5*8)+(4*4)+(3*8)+(2*4)+(1*6)=112
112 % 10 = 2
So 3848-46-2 is a valid CAS Registry Number.

3848-46-2Downstream Products

3848-46-2Relevant academic research and scientific papers

A novel and efficient strategy for the synthesis of various carbamates using carbamoyl chlorides under solvent-free and grinding conditions using microwave irradiation

Zare, Hassan,Ghanbari, Mohammad Mehdi,Jamali, Marzieh,Aboodi, Abdollah

experimental part, p. 883 - 886 (2012/08/28)

We present an efficient, fast and simple strategy of generating the intermediate carbamoyl chlorides from secondary amines using stoichiometric amounts of bis(trichloromethyl)carbonate (BTC) in solution and solvent-free conditions with excellent yields. The results obtained showed the yield increasing on whether a base was used. Finally, an efficient and rapid synthesis of variety carbamate derivatives was developed by the reaction with a high variety of different alcohols, phenols, diols and this intermediate at room temperature with grinding and in solvent-free conditions under microwave irradiation. The presence of various safe bases is shown to be effective in reducing the reaction times, increasing the yields and easing purification. The present method does not involve any hazardous phosgene.

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