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6047-01-4

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6047-01-4 Usage

General Description

Cytisine hydrochloride is a chemical compound that is derived from the Cytisus laburnum plant and has been used as a smoking cessation aid. It acts as a partial agonist at nicotinic acetylcholine receptors, leading to a reduction in the craving for nicotine and withdrawal symptoms in individuals trying to quit smoking. Cytisine hydrochloride has been found to be effective in helping people quit smoking and has been approved for this purpose in various European countries. It is also being studied for its potential anti-tumor and antiviral properties. However,

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 articles and documents

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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