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Cytisine hydrochloride is a chemical compound derived from the Cytisus laburnum plant, known for its efficacy as a smoking cessation aid. It functions as a partial agonist at nicotinic acetylcholine receptors, which helps to diminish nicotine cravings and alleviate withdrawal symptoms in individuals attempting to quit smoking. With its potential anti-tumor and antiviral properties, cytisine hydrochloride is a subject of ongoing research and has been approved for smoking cessation in several European countries.

6047-01-4

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6047-01-4 Usage

Uses

Used in Pharmaceutical Industry:
Cytisine hydrochloride is used as a smoking cessation aid for its ability to reduce nicotine cravings and withdrawal symptoms, aiding individuals in their efforts to quit smoking.
Used in Research and Development:
Cytisine hydrochloride is used as a subject of research for its potential anti-tumor properties, with ongoing studies exploring its effects on various types of cancer.
Used in Antiviral Research:
Cytisine hydrochloride is also being studied for its potential antiviral properties, with research aimed at understanding its impact on viral infections and possible therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6047-01-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,4 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6047-01:
(6*6)+(5*0)+(4*4)+(3*7)+(2*0)+(1*1)=74
74 % 10 = 4
So 6047-01-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2O.ClH/c14-11-3-1-2-10-9-4-8(5-12-6-9)7-13(10)11;/h1-3,8-9,12H,4-7H2;1H/t8-,9+;/m0./s1

6047-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-amino-1H-pyrimidin-2-one,hydrochloride

1.2 Other means of identification

Product number -
Other names 6-Aminopyrimidin-2(1H)-one hydrochloride

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:6047-01-4 SDS

6047-01-4Downstream Products

6047-01-4Relevant academic research and scientific papers

A short synthesis of (±)-cytisine

Botuha, Candice,Galley, Carl M. S.,Gallagher, Timothy

, p. 1825 - 1826 (2007/10/03)

The synthesis of racemic cytisine 1 has been completed using (i) N-selective alkylation of 6-bromopyridone with bromide 6 and (ii) Pd(o) mediated intramolecular a-arylation of lactam 8 as key steps to achieve rapid assembly of the tricyclic core skeleton of the lupin alkaloids.

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