1228569-39-8 Usage
General Description
(S)-2-(1-aminoethyl)-4-chlorophenol is a chemical compound with the molecular formula C8H10ClNO. It is a chiral compound, with the (S)-enantiomer being the biologically active form. (S)-2-(1-aMinoethyl)-4-chlorophenol has both an amine functional group and a phenol functional group, which gives it potential use in various pharmaceutical applications. Its properties and structure make it suitable for use as a building block in the synthesis of a variety of organic molecules. Additionally, its chlorophenol structure gives it potential as an anti-bacterial agent in certain applications. Overall, (S)-2-(1-aminoethyl)-4-chlorophenol has potential as a versatile building block for the synthesis of pharmaceuticals and other organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 1228569-39-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,5,6 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1228569-39:
(9*1)+(8*2)+(7*2)+(6*8)+(5*5)+(4*6)+(3*9)+(2*3)+(1*9)=178
178 % 10 = 8
So 1228569-39-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H3Cl3N2/c9-4-1-2-6-5(3-4)7(10)13-8(11)12-6/h1-3H
1228569-39-8Relevant 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
