1228571-53-6 Usage
General Description
"(R)-2-(1-aMinoethyl)-4-chlorophenol" is a synthetic compound that belongs to the class of organic compounds known as phenols. Phenols are compounds containing a phenolic ring, which consists of a benzene ring with a hydroxyl group. The "R" in its name denotes the chirality of the carbon atom carrying the aminoethyl group. This particular compound contains a chlorine atom attached to the benzene ring and is also characterized by an aminoethyl group on the second position of the ring. In the context of this compound, the 1-aminoethyl group suggests that the nitrogen atom is directly bonded to the carbon atom in the side chain. The chemical properties, interactions, uses and effects of this compound can vary and are subject to investigation.
Check Digit Verification of cas no
The CAS Registry Mumber 1228571-53-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,5,7 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1228571-53:
(9*1)+(8*2)+(7*2)+(6*8)+(5*5)+(4*7)+(3*1)+(2*5)+(1*3)=156
156 % 10 = 6
So 1228571-53-6 is a valid CAS Registry Number.
1228571-53-6Relevant articles and documents
Design and synthesis of chiral oxathiozinone scaffolds: Efficient synthesis of hindered enantiopure sulfinamides and sulfinyl ketimines
Han, Zhengxu S.,Herbage, Melissa A.,Mangunuru, Hari P. R.,Xu, Yibo,Zhang, Li,Reeves, Jonathan T.,Sieber, Joshua D.,Li, Zhibin,Decroos, Philomen,Zhang, Yongda,Li, Guisheng,Li, Ning,Ma, Shengli,Grinberg, Nelu,Wang, Xiaojun,Goyal, Navneet,Krishnamurthy, Dhileep,Lu, Bruce,Song, Jinhua J.,Wang, Guijun,Senanayake, Chris H.
supporting information, p. 6713 - 6717 (2013/07/26)
Is that S-O? The title scaffolds have a highly active and properly differentiated S-O bond for the efficient synthesis of enantiopure sulfinamides. The method is practical, green, and has the potential to provide an economical commercial process for the synthesis of bulky sulfinamides. Copyright