22906-75-8 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
3,5-dimethylpyrazole-1-carboxamidine is utilized as a key intermediate in the creation of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides due to its versatile chemical structure and reactivity.
Used in Organic Chemistry:
In the field of organic chemistry, 3,5-dimethylpyrazole-1-carboxamidine serves as a valuable component in the synthesis of complex organic molecules, leveraging its unique functional group for reactions and transformations.
Used in Medicinal Chemistry:
3,5-dimethylpyrazole-1-carboxamidine is employed as a precursor in medicinal chemistry for the design and synthesis of potential therapeutic agents, capitalizing on its capacity to be modified and incorporated into bioactive molecules.
Used in Biochemistry:
3,5-dimethylpyrazole-1-carboxamidine is also used in biochemistry for the exploration of its interactions with biological systems, potentially leading to insights into its pharmacological properties and applications in drug discovery.
The potential uses of 3,5-dimethylpyrazole-1-carboxamidine are still under investigation, indicating a promising future for 3,5-dimethylpyrazole-1-carboxamidine in scientific research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 22906-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,0 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22906-75:
(7*2)+(6*2)+(5*9)+(4*0)+(3*6)+(2*7)+(1*5)=108
108 % 10 = 8
So 22906-75-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H12N4.ClH/c1-4-5(2)10-11(6(4)3)7(8)9;/h1-3H3,(H3,8,9);1H
22906-75-8Relevant academic research and scientific papers
Improved Method for the Preparation of Guanidines
Kim, Kyoung Soon,Qian, Ligang
, p. 7677 - 7680 (2007/10/02)
Use of N,N'-di-(tert-butoxycarbonyl)thiourea 1 in the presence of mercuric chloride provides a very efficient method for the bis-Boc protected guanidine formation of the amino compounds which are highly deactivated either sterically or electronically.
