21602-66-4 Usage
Description
1-(1-(2-thienyl)cyclohexyl)morpholine is a chemical compound characterized by its unique structure, which includes a cyclohexyl ring connected to a thiophene group and a morpholine moiety. 1-(1-(2-thienyl)cyclohexyl)morpholine is known for its potential medicinal properties and has been studied for various therapeutic effects, including antiparasitic, anti-inflammatory, and analgesic actions. It also exhibits antifungal and antibacterial activities, making it a versatile compound with applications in multiple fields.
Uses
Used in Pharmaceutical Industry:
1-(1-(2-thienyl)cyclohexyl)morpholine is used as a building block for the synthesis of various pharmaceuticals due to its potential medicinal properties and diverse therapeutic effects, such as antiparasitic, anti-inflammatory, and analgesic actions.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(1-(2-thienyl)cyclohexyl)morpholine is used as a component in the development of new agrochemicals, leveraging its antifungal and antibacterial activities to create more effective products for agricultural use.
Used in Materials Science:
1-(1-(2-thienyl)cyclohexyl)morpholine is used as a precursor in the production of novel materials and polymers, taking advantage of its unique cyclohexyl-thiophene-morpholine structure to create innovative materials with potential applications in various industries.
Overall, 1-(1-(2-thienyl)cyclohexyl)morpholine is a versatile chemical compound with a wide range of potential applications in the fields of medicine, agriculture, and materials science, making it a valuable asset for researchers and developers in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 21602-66-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,0 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21602-66:
(7*2)+(6*1)+(5*6)+(4*0)+(3*2)+(2*6)+(1*6)=74
74 % 10 = 4
So 21602-66-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H21NOS.ClH/c1-2-6-14(7-3-1,13-5-4-12-17-13)15-8-10-16-11-9-15;/h4-5,12H,1-3,6-11H2;1H
21602-66-4Relevant articles and documents
Preparation of tertiary alkyl carbinamines, propargylamines, and α-heteroarylamines by ketone-based aminoalkylation
Katritzky, Alan R.,Yang, Hongfang,Singh, Sandeep K.
, p. 286 - 290 (2007/10/03)
(Chemical Equation Presented). Ketones 6a-i were converted into their benzotriazolylamine adducts 8a-i either directly from the corresponding ketone 6a or via enamines 7b-i. Adducts 8a-i on treatment with Grignard reagents, lithium phenylacetylide, or heteroaryllithiums gave tertiary alkyl carbinamines 9a-h (47-61%), propargylamines 10a-i (30-98%), and α-heteroarylamines 11a-k (44-85%), respectively.
Carbon-13 nuclear magnetic resonance spectra of phenycyclidine analogs
Brine,Williams,Boldt,Carroll
, p. 1425 - 1429 (2007/10/05)
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