19210-21-0 Usage
Description
(S)-(+)-2-Chloropropan-1-ol, also known as Chloro-1-propanol, is a chiral organic compound with a clear colorless to slightly yellow liquid appearance. It is characterized by its unique stereochemistry, where the chlorine atom is attached to the second carbon of the propane molecule, and the hydroxyl group is attached to the first carbon. (S)-(+)-2-Chloropropan-1-ol exhibits specific chemical properties that make it suitable for various applications.
Uses
Used in Pharmaceutical Industry:
(S)-(+)-2-Chloropropan-1-ol is used as an active pharmaceutical ingredient for the treatment of cardiovascular diseases. Its unique chemical structure allows it to interact with specific biological targets, providing therapeutic benefits in managing and treating heart-related conditions.
Used in Chemical Synthesis:
(S)-(+)-2-Chloropropan-1-ol can also be used as a key intermediate in the synthesis of various organic compounds. Its versatile functional groups enable it to participate in a wide range of chemical reactions, making it a valuable building block for the production of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
Due to its unique stereochemistry and chemical properties, (S)-(+)-2-Chloropropan-1-ol is utilized in research and development for the study of chiral compounds and their applications in various fields. It serves as a valuable tool for understanding the role of stereochemistry in biological systems and the development of enantioselective synthetic methods.
Check Digit Verification of cas no
The CAS Registry Mumber 19210-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,1 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19210-21:
(7*1)+(6*9)+(5*2)+(4*1)+(3*0)+(2*2)+(1*1)=80
80 % 10 = 0
So 19210-21-0 is a valid CAS Registry Number.
InChI:InChI=1/C3H7ClO/c1-3(4)2-5/h3,5H,2H2,1H3/t3-/m0/s1
19210-21-0Relevant articles and documents
Oxidation of olefins by palladium(II): Part 17. An asymmetric chlorohydrin synthesis catalyzed by a bimetallic palladium(II) complex
El-Qisairi, Arab,Henry, Patrick M.
, p. 50 - 60 (2007/10/03)
Previous studies showed that oxidation of α-olefins with monometallic catalysts containing chiral diphosphines and diamines gave chlorohydrins with poor to good enantioselectivites (28-82% ee). The present studies demonstrate that bimetallic catalysts containing a β-triketone and bridging chiral diphosphine and diamines are excellent catalysts for this reaction giving enantioselectivites considerably higher than the monometallic catalysts. Enantioselectivities were more than 50% for most olefins tested. The highest optical purities were 94% ee for propene and 93% ee for allylphenyl ether. A useful feature of this asymmetric synthesis is the fact it is a net air oxidation.
