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1-(2-Hydrazinylethyl)piperidine, also known as NEPA, is a chemical compound with the molecular formula C8H18N2. It is a novel antiemetic drug that is used to prevent chemotherapy-induced nausea and vomiting. NEPA is a combination of netupitant, a neurokinin-1 receptor antagonist, and palonosetron, a serotonin 5-HT3 receptor antagonist. This dual mechanism of action makes NEPA highly effective in preventing nausea and vomiting associated with chemotherapy.

6979-01-7

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6979-01-7 Usage

Uses

Used in Pharmaceutical Industry:
1-(2-Hydrazinylethyl)piperidine is used as an antiemetic agent for preventing chemotherapy-induced nausea and vomiting. Its dual mechanism of action, combining the effects of a neurokinin-1 receptor antagonist and a serotonin 5-HT3 receptor antagonist, makes it highly effective in managing these side effects. NEPA is well-tolerated and has shown to be more effective than traditional antiemetic drugs, making it a promising option for cancer patients undergoing chemotherapy.

Check Digit Verification of cas no

The CAS Registry Mumber 6979-01-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6979-01:
(6*6)+(5*9)+(4*7)+(3*9)+(2*0)+(1*1)=137
137 % 10 = 7
So 6979-01-7 is a valid CAS Registry Number.

6979-01-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-piperidin-1-ylethylhydrazine

1.2 Other means of identification

Product number -
Other names 1-(2-hydrazinylethyl)piperidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6979-01-7 SDS

6979-01-7Downstream Products

6979-01-7Relevant academic research and scientific papers

2-Pyrazolin-5-ones bearing a basic dialkylaminoalkyl substituent at the N1-position: Preparation and NMR spectroscopic investigations

Wolf, Barbara M.T.,Eller, Gernot A.,Holzer, Wolfgang

experimental part, p. 2035 - 2042 (2009/04/06)

2-Pyrazolin-5-ones (= tautomers to 5-hydroxypyrazols) bearing dialkylaminoyalkyl substituents at the ring nitrogen atom N-1 are prepared from the corresponding hydrazines and beta-ketoesters. Detailed NMR spectroscopic investigations (1H,

Synthesis of 9,10-anthraquinone monoalkylaminoalkylhydrazones as potential antitumor drugs

Antonini,Polucci,Cola,Palmieri,Martelli,Bontemps-Gracz

, p. 1641 - 1648 (2007/10/02)

In the constant search for new compounds endowed with antitumor activity we have synthesized a series of anthraquinone hydrazones, which can be seen either as opened-cycle modified anthrapyrazoles or as chromophore-modified anthracenediones. Seven 9,10-anthraquinone monoalkylaminoalkylhydrazones (3c-i) were synthesized from 10,10-dibromoanthrone (4) and a suitable N-alkylhydrazine. The hydrazones were converted into hydrochlorides and tested for their cytotoxic activity against L1210 murine leukemia cells. Two of them possess marginal activity in vitro.

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