83467-28-1 Usage
Uses
Used in Chemical Synthesis:
4-(2-Bromo-ethyl)-3,5-dimethyl-1H-pyrazole is used as an intermediate in the synthesis of various organic compounds for research and development purposes. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable component in the creation of new molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-(2-Bromo-ethyl)-3,5-dimethyl-1H-pyrazole is used as a building block for the development of potential drug candidates. Its structure may contribute to the design of new therapeutic agents, with its properties being tailored to target specific biological pathways or receptors.
Used in Laboratory Applications:
4-(2-Bromo-ethyl)-3,5-dimethyl-1H-pyrazole is employed in various laboratory settings for educational purposes, as well as for conducting experiments that explore its reactivity, stability, and potential interactions with other compounds. This helps researchers gain a deeper understanding of its properties and potential applications.
Used in Material Science:
In the field of material science, 4-(2-Bromo-ethyl)-3,5-dimethyl-1H-pyrazole may be used to develop new materials with specific properties, such as improved thermal stability or chemical resistance. Its incorporation into polymers or other materials could lead to advancements in various industries, including electronics, automotive, and aerospace.
Check Digit Verification of cas no
The CAS Registry Mumber 83467-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,6 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83467-28:
(7*8)+(6*3)+(5*4)+(4*6)+(3*7)+(2*2)+(1*8)=151
151 % 10 = 1
So 83467-28-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H11BrN2/c1-5-7(3-4-8)6(2)10-9-5/h3-4H2,1-2H3,(H,9,10)
83467-28-1Relevant academic research and scientific papers
Synthesis and structural characterization of (CH2)n-bridged indenyl-pyrazoles and their cyclopentadienyl nickel(II) complexes
Tan, Weiqiang,Yu, Zhengkun,Liu, Bing,Wu, Kaikai,Liu, Zishuang,Chen, Jinzhu
scheme or table, p. 199 - 206 (2009/04/13)
A new class of (CH2)n-bridged indenyl-pyrazoles [4-{Ind-(CH2)n}-RR′PzH] (Ind = 1H-inden-3-yl, n = 1-3, RR′Pz = 3,5-disubstituted pyrazolato) were synthesized. Reactions of the indenyl-functionalized pyrazoles wi
REARRANGEMENTS AND CYCLIZATIONS - XIV. RING-OPENING REACTIONS OF 1,1-DIACETYLCYCLOPROPANE WITH HYDRAZINE AND HYDROXYLAMINE DERIVATIVES AS THE NOVEL SYNTHESIS OF Β-X-ETHYL SUBSTITUTED PYRAZOLES AND ISOXAZOLES
Zefirov, Nikolai S.,Kozhushkov, Sergei I.,Kuznetsova, Tamara S.
, p. 1693 - 1697 (2007/10/02)
The reactions of 1,1-diacetylcyclopropane (1) with a number of hydrazine and hydroxylamine derivatives proceed via cyclopropane ring opening with incorporation of external nucleophile (solvent) to give the 4-β-X-ethyl derivatives of 3,5-dimethylpyrazoles
