6007-66-5 Usage
General Description
N-(2-Hydroxypropyl) thiomorpholine is a chemical compound that is used in various industrial applications, such as in the production of pharmaceuticals, adhesives, and plastics. It is a versatile compound with antimicrobial properties, making it suitable for use in personal care products and as a preservative in various formulations. N-(2-Hydroxypropyl) thiomorpholine is also used as a corrosion inhibitor in metalworking fluids and as a stabilizer in rubber production. Its ability to react with various organic compounds makes it a valuable building block for the synthesis of other chemicals. Overall, N-(2-Hydroxypropyl) thiomorpholine is a useful and multifunctional chemical with a wide range of applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 6007-66-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6007-66:
(6*6)+(5*0)+(4*0)+(3*7)+(2*6)+(1*6)=75
75 % 10 = 5
So 6007-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NOS/c9-5-1-2-8-3-6-10-7-4-8/h9H,1-7H2
6007-66-5Relevant articles and documents
Manganese-Catalyzed Anti-Markovnikov Hydroamination of Allyl Alcohols via Hydrogen-Borrowing Catalysis
Das, Kuhali,Sarkar, Koushik,Maji, Biplab
, p. 7060 - 7069 (2021/06/30)
Controlling the selectivity in a hydroamination reaction is an extremely challenging yet highly desirable task for the diversification of amines. In this article, a selective formal anti-Markovnikov hydroamination of allyl alcohols is presented. It enables the versatile synthesis of valuable γ-amino alcohol building blocks. A phosphine-free Earth's abundant manganese(I) complex catalyzed the reaction under hydrogen-borrowing conditions. A vast range of aliphatic, aromatic amines, drug molecules, and natural product derivatives underwent successful hydroamination with primary and secondary allylic alcohols with excellent functional group tolerance (57 examples). The catalysis could be performed on a gram scale and has been applied for the synthesis of drug molecules. The mechanistic studies revealed the metal-ligand bifunctionality as well as hemilability of the ligand backbone as the key design principle for the success of this catalysis.