1049809-90-6 Usage
Description
(S)-4-(3-chloropropyl)-3-methylmorpholine is a chiral chemical compound characterized by a morpholine ring with a 3-methyl group and a 3-chloropropyl group attached to it. As a chiral molecule, it possesses a non-superimposable mirror image and exists in two enantiomeric forms, specifically (S)and (R)-. (S)-4-(3-chloropropyl)-3-methylmorpholine is notable for its reactivity due to the chloropropyl group, which makes it a versatile intermediate in the synthesis of a wide range of products.
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
(S)-4-(3-chloropropyl)-3-methylmorpholine is utilized as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and reactivity allow for the creation of complex molecules with potential therapeutic or pesticidal properties.
Used in Surfactant Production:
(S)-4-(3-chloropropyl)-3-methylmorpholine serves as a building block in the production of surfactants, which are essential in a variety of industries for their ability to reduce surface tension between liquids and solids. Its incorporation into surfactants can enhance their performance characteristics, such as solubility and foaming properties.
Used in Polymer Production:
(S)-4-(3-chloropropyl)-3-methylmorpholine is also used in the synthesis of polymers, contributing to the development of materials with specific properties tailored for various applications, such as plastics, coatings, and adhesives.
Used in Organic Synthesis as a Building Block:
In the realm of organic synthesis, (S)-4-(3-chloropropyl)-3-methylmorpholine is employed as a versatile building block to construct a diverse array of chemical structures. Its presence in these structures can impart novel properties and functionalities, expanding the scope of chemical compounds available for research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1049809-90-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,9,8,0 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1049809-90:
(9*1)+(8*0)+(7*4)+(6*9)+(5*8)+(4*0)+(3*9)+(2*9)+(1*0)=176
176 % 10 = 6
So 1049809-90-6 is a valid CAS Registry Number.
1049809-90-6Relevant articles and documents
Practical synthesis of a cathepsin S Inhibitor: Route identification, purification strategies, and serendipitous discovery of a crystalline salt form
Deng, Xiaoliu,Liang, Jimmy T.,Peterson, Matthew,Rynberg, Raymond,Cheung, Eugene,Mani, Neelakandha S.
experimental part, p. 1940 - 1947 (2010/05/18)
Chemical Equation Presented A redox economical strategy resulted in a concise, modular synthesis of compound 1, a potent Cathepsin S inhibitor. Starting from three building blocks, crude drug substance was prepared, in a two-step sequence in high yield. Efficient purification of the crude drug substance was accomplished via the formation of an unusual monoethyl oxalate salt.
CARBON-LINKED TETRAHYDRO-PYRAZOLO-PYRIDINE MODULATORS OF CATHEPSIN S
-
Page/Page column 63, (2008/12/08)
Carbon-linked tetrahydro-pyrazolo-pyridine compounds are described, which are useful as cathepsin S modulators. Such compounds may be used in pharmaceutical compositions and methods for the treatment of disease states, disorders, and conditions mediated by cathepsin S activity, such as psoriasis, pain, multiple sclerosis, atherosclerosis, and rheumatoid arthritis.
