65686-13-7 Usage
General Description
2-(4-Chloro-phenoxy)ethyl methyl amine is a chemical compound used in the synthesis of pharmaceuticals and agrochemicals. It is an organic compound composed of a chlorophenyl group, an ethyl group, and a methylamine group. 2-(4-CHLORO-PHENOXY)ETHYL METHYL AMINE has various potential applications in the manufacturing of pharmaceuticals and agricultural products due to its specific chemical properties. It is commonly used as an intermediate in the production of various active pharmaceutical ingredients and as a starting material in the synthesis of agrochemicals. The compound is also utilized in research and development projects in the pharmaceutical and agricultural industries.
Check Digit Verification of cas no
The CAS Registry Mumber 65686-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,8 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65686-13:
(7*6)+(6*5)+(5*6)+(4*8)+(3*6)+(2*1)+(1*3)=157
157 % 10 = 7
So 65686-13-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H12ClNO/c1-11-6-7-12-9-4-2-8(10)3-5-9/h2-5,11H,6-7H2,1H3/p+1
65686-13-7Relevant articles and documents
Convenient Continuous Flow Synthesis of N-Methyl Secondary Amines from Alkyl Mesylates and Epoxides
Lebel, Hélène,Mathieu, Gary,Patel, Heena
, p. 2157 - 2168 (2020/11/23)
The first continuous flow process was developed to synthesize N-methyl secondary amines from alkyl mesylates and epoxides via a nucleophilic substitution using aqueous methylamine. A variety of N-methyl secondary amines were produced in good to excellent yields, including a number of bioactive compounds or their precursors. Up to 10.6 g (88% yield) of an N-methyl secondary amine was produced in 140 min process time. The amination procedure included an in-line workup, and the starting mesylate material was also produced in continuous flow from the corresponding alcohol. Finally, an in-line process combining the mesylate synthesis and nucleophilic substitution was developed.
