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N-Phenyl-phenaethylcarbaminsaeure-chlorid, also known as N-phenyl-phenethylcarbamic acid chloride, is an organic compound with the chemical formula C14H12ClNO2. It is a derivative of phenethylamine, featuring a carbamic acid chloride functional group and a phenyl ring attached to the nitrogen atom. N-Phenyl-phenaethylcarbaminsaeure-chlorid is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other psychoactive substances. Due to its reactivity, it is essential to handle N-Phenyl-phenaethylcarbaminsaeure-chlorid with care, following proper safety protocols and guidelines.

7001-94-7

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7001-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7001-94-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,0 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7001-94:
(6*7)+(5*0)+(4*0)+(3*1)+(2*9)+(1*4)=67
67 % 10 = 7
So 7001-94-7 is a valid CAS Registry Number.

7001-94-7Relevant academic research and scientific papers

Discovery of novel quaternary ammonium derivatives of (3R)-quinuclidinyl carbamates as potent and long acting muscarinic antagonists

Prat, Maria,Buil, María Antonia,Fernández, Maria Dolors,Castro, Jordi,Monleón, Juan Manuel,Tort, Laia,Casals, Gaspar,Ferrer, Manuel,Huerta, Josep Maria,Espinosa, Snia,López, Manuel,Segarra, Victor,Gavald, Amadeu,Miralpeix, Montserrat,Ramos, Israel,Vilella, Dolors,González, Marisa,Córdoba, Mnica,Cárdenas, Alvaro,Antón, Francisca,Beleta, Jorge,Ryder, Hamish

, p. 3457 - 3461 (2011/06/24)

Novel quaternary ammonium derivatives of N,N-disubstituted (3R)-quinuclidinyl carbamates have been identified as potent M3 muscarinic antagonists with long duration of action in an in vivo model of bronchoconstriction. These compounds have also presented a high level of metabolic transformation (human liver microsomes). The synthesis, structure-activity relationships and biological evaluation of these compounds are reported.

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