10113-37-8 Usage
General Description
N-(2-chloro-6-methylphenyl)formamide is a chemical compound that belongs to the class of formamides, which are derivatives of formic acid. It is composed of a formyl group attached to a phenyl ring that has a chlorine atom at position 2 and a methyl group at position 6. N-(2-CHLORO-6-METHYLPHENYL)FORMAMIDE& is commonly used in organic synthesis and pharmaceutical research as a building block for the preparation of various biologically active molecules. It may also have potential applications in the development of agrochemicals and materials science. However, it is important to handle this chemical with caution as it may have harmful effects on human health and the environment if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 10113-37-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,1 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10113-37:
(7*1)+(6*0)+(5*1)+(4*1)+(3*3)+(2*3)+(1*7)=38
38 % 10 = 8
So 10113-37-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClNO/c1-6-3-2-4-7(9)8(6)10-5-11/h2-5H,1H3,(H,10,11)
10113-37-8Relevant articles and documents
Enantioselective Synthesis of Azetidines through [3 + 1]-Cycloaddition of Donor-Acceptor Aziridines with Isocyanides
Zhang, Fengcai,Sang, Xinpeng,Zhou, Yuqiao,Cao, Weidi,Feng, Xiaoming
supporting information, p. 1513 - 1517 (2022/03/01)
The enantioselective [3 + 1]-cycloaddition of racemic donor-acceptor (D-A) aziridines with isocyanides was first realized under mild reaction conditions using a chiral N,N′-dioxide/MgIIcomplex as catalyst, providing a facile route to enantioenriched exo-imido azetidines with good to excellent yield (up to 99%) and enantioselectivity (up to 94% ee). An obvious chiral amplification effect was observed in this system, and an explanation was elucidated based on the experimental investigation and X-ray crystal structure of the enantiomerically pure catalyst.
