18915-87-2 Usage
Description
1-(butylsulfanyl)-3-chloropropan-2-ol is a chemical compound with the molecular formula C7H15ClOS. It is a derivative of chloropropanol, characterized by the presence of a sulfur atom bonded to a butyl group, a chlorine atom, and a hydroxyl group. 1-(butylsulfanyl)-3-chloropropan-2-ol is known for its anesthetic and sedative properties, and it holds potential in various fields of research and industry due to its unique structural features and reactivity.
Uses
Used in Pharmaceutical Industry:
1-(butylsulfanyl)-3-chloropropan-2-ol is used as an intermediate compound for the synthesis of various pharmaceuticals. Its anesthetic and sedative properties make it a valuable component in the development of medications aimed at treating pain and anxiety.
Used in Pesticide Industry:
In the pesticide industry, 1-(butylsulfanyl)-3-chloropropan-2-ol is used as a key component in the formulation of certain pesticides. Its unique chemical structure allows it to target specific pests while minimizing harm to the environment and non-target organisms.
Used in Industrial Chemicals:
1-(butylsulfanyl)-3-chloropropan-2-ol is also utilized in the production of other industrial chemicals, where its specific reactivity and biological activity can be harnessed for various applications, such as in the manufacturing of solvents, detergents, and additives.
Check Digit Verification of cas no
The CAS Registry Mumber 18915-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,1 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18915-87:
(7*1)+(6*8)+(5*9)+(4*1)+(3*5)+(2*8)+(1*7)=142
142 % 10 = 2
So 18915-87-2 is a valid CAS Registry Number.
18915-87-2Relevant articles and documents
Synthesis and characterisation of thioether functionalised gallium and indium alkoxides
Barth, Sven,Biegger, Felix,Puchberger, Michael
supporting information, p. 16439 - 16445 (2015/09/28)
This paper provides evidence of formerly unknown thioether coordination in metal alkoxides. The thioether functionalised alkanols serving as alcoholate ligands have been prepared by a generic route. The gallium and indium alkoxides provide the first evidence for sulphur coordination in the liquid and solid state in metal alkoxide derivatives. The presence of amines suppresses the coordination of thioether moieties leading to a well-known bonding mode in aminoalcoholates.
