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C6H7N3OClH is a chemical compound composed of carbon, hydrogen, nitrogen, oxygen, and chlorine atoms. It is a hydrochloride salt, indicated by the presence of chlorine, and may be an amine or an amide due to the presence of nitrogen. The specific properties and characteristics of C6H7N3O*ClH are dependent on its exact molecular structure and the bonding of its constituent atoms. Without further information, it is challenging to provide more details about its properties or uses.

1154063-17-8

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1154063-17-8 Usage

Uses

Given the limited information about the compound, it is not possible to list specific applications for C6H7N3OClH. However, based on the presence of various elements, we can hypothesize potential uses in different industries:
Used in Pharmaceutical Industry:
C6H7N3OClH could be used as an active pharmaceutical ingredient for [application reason], given its potential as an amine or amide, which are common in drug development.
Used in Chemical Industry:
In the chemical industry, C6H7N3OClH might be used as a reagent or intermediate in the synthesis of other compounds, due to its diverse functional groups.
Used in Research and Development:
C6H7N3OClH could be utilized as a research compound for studying its properties and potential applications in various fields, such as material science or biochemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1154063-17-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,4,0,6 and 3 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1154063-17:
(9*1)+(8*1)+(7*5)+(6*4)+(5*0)+(4*6)+(3*3)+(2*1)+(1*7)=118
118 % 10 = 8
So 1154063-17-8 is a valid CAS Registry Number.

1154063-17-8Downstream Products

1154063-17-8Relevant academic research and scientific papers

Discovery of substituted 2,4,4-triarylimidazoline derivatives as potent and selective neuropeptide Y Y5 receptor antagonists

Sato, Nagaaki,Jitsuoka, Makoto,Ishikawa, Shiho,Nagai, Keita,Tsuge, Hiroyasu,Ando, Makoto,Okamoto, Osamu,Iwaasa, Hisashi,Gomori, Akira,Ishihara, Akane,Kanatani, Akio,Fukami, Takehiro

scheme or table, p. 1670 - 1674 (2009/11/30)

Novel imidazoline derivatives were discovered to be potent neuropeptide Y Y5 receptor antagonists. High-throughput screening of Merck sample collections against the human Y5 receptor resulted in the identification of 2,4,4-triphenylimidazoline (1), which had an IC50 of 54 nM. Subsequent optimization led to the identification of several potent derivatives.

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