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PHENETHYL-HYDRAZINE HYDROCHLORIDE is a hydrazine derivative featuring a phenethyl substituent, commonly utilized in scientific research and pharmaceutical applications. Its hydrochloride salt form enhances solubility and ease of handling, making it a valuable tool for studying neurotransmitter systems in the brain and developing potential therapies for neurological disorders. However, its toxic and potentially hazardous nature necessitates careful handling and use.

5470-36-0

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5470-36-0 Usage

Uses

Used in Scientific Research:
PHENETHYL-HYDRAZINE HYDROCHLORIDE is used as a research chemical for studying the nervous system due to its effects on neurotransmitter systems in the brain.
Used in Pharmaceutical Applications:
PHENETHYL-HYDRAZINE HYDROCHLORIDE is used as a precursor in the development of potential therapies for neurological disorders, given its potential as a neurotoxin and its impact on brain neurotransmitter systems.

Check Digit Verification of cas no

The CAS Registry Mumber 5470-36-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,7 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5470-36:
(6*5)+(5*4)+(4*7)+(3*0)+(2*3)+(1*6)=90
90 % 10 = 0
So 5470-36-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2.ClH/c9-10-7-6-8-4-2-1-3-5-8;/h1-5,10H,6-7,9H2;1H

5470-36-0Upstream product

5470-36-0Relevant academic research and scientific papers

PYRAZOLOPYRAZINES AND THEIR USE IN THE TREATMENT, AMELIORATION OR PREVENTION OF A VIRAL DISEASE

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Page/Page column 37; 38, (2017/04/11)

The present invention relates to a compound having the general formula (IIa) or (IIb), optionally in the form of a pharmaceutically acceptable salt, solvate, polymorph,codrug, cocrystal,prodrug, tautomer, racemate, enantiomer, or diastereomer or mixture thereof, which are useful in treating, ameloriating or preventing a viral disease. Furthermore, specific combination therapies are disclosed.

A variation of the Fischer indolization involving condensation of quinone monoketals and aliphatic hydrazines

Zhang, Jinzhu,Yin, Zhiwei,Leonard, Patrick,Wu, Jing,Sioson, Kate,Liu, Che,Lapo, Robert,Zheng, Shengping

supporting information, p. 1753 - 1757,5 (2013/04/10)

A new twist: A one-pot nitrous acid free, diazonium-free, and transition-metal-free variation of the Fischer indole synthesis has been developed. Condensation of quinone monoketals and aliphatic hydrazine hydrochlorides afforded indoles via intermediate alkylaryldiazenes. This method will complement the classical Fischer indole synthesis by providing indoles in two steps from widely available phenols under mild conditions. Copyright

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