869967-21-5 Usage
Uses
Used in Pharmaceutical Industry:
4-METHYL-1-TRITYL-1H-IMIDAZOLE-2-CARBALDEHYDE is used as a reagent in organic synthesis for the production of pharmaceuticals. Its ability to form complex molecular structures makes it instrumental in the development of new drugs and medicinal compounds.
Used in Fine Chemicals Industry:
In the fine chemicals industry, 4-METHYL-1-TRITYL-1H-IMIDAZOLE-2-CARBALDEHYDE is utilized as a reagent for the synthesis of specialty chemicals. Its unique properties contribute to the creation of high-quality products with specific applications in various fields.
Used in Medicinal Chemistry Research:
4-METHYL-1-TRITYL-1H-IMIDAZOLE-2-CARBALDEHYDE is employed as a research tool in medicinal chemistry. Its role as a versatile building block aids scientists in exploring new chemical pathways and developing innovative therapeutic agents.
Used in Chemical Research:
4-METHYL-1-TRITYL-1H-IMIDAZOLE-2-CARBALDEHYDE is also used in broader chemical research to study the properties and reactions of imidazole derivatives and trityl groups. Its presence in experiments can provide insights into the behavior of similar compounds and contribute to the advancement of chemical knowledge.
Check Digit Verification of cas no
The CAS Registry Mumber 869967-21-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,9,6 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 869967-21:
(8*8)+(7*6)+(6*9)+(5*9)+(4*6)+(3*7)+(2*2)+(1*1)=255
255 % 10 = 5
So 869967-21-5 is a valid CAS Registry Number.
869967-21-5Relevant articles and documents
LRRK2 INHIBITORS
-
, (2013/02/28)
Provided herein are compounds that inhibit or partially inhibit the activity of leucine rich repeat kinases. Also provided herein are methods of treatment of CNS disorders comprising administration of inhibitors of leucine rich repeat kinases.
Monocyclic, substituted imidazoles as glycosidase inhibitors
Magdolen, Peter,Vasella, Andrea
, p. 2454 - 2469 (2007/10/03)
A range of 4-monosubstituted and 2,4-disubstituted 1H-imidazoles and 1H-imidazole-1-ethanols (R-C(4): CH2CH2Ph, CHOHCH 2Ph, Ph, or Me; R-C(2): CH2OH, CHOHCH2OH, CN, or CH2NHAc) were prepare