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29228-83-9

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29228-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29228-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,2 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29228-83:
(7*2)+(6*9)+(5*2)+(4*2)+(3*8)+(2*8)+(1*3)=129
129 % 10 = 9
So 29228-83-9 is a valid CAS Registry Number.

29228-83-9SDS

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-methyl-5-(piperidin-1-ylmethyl)-2-sulfanylidene-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 6-Methyl-5-piperidinomethyl-2-thioxo-2,3-dihydro-1H-pyrimidin-4-on

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:29228-83-9 SDS

29228-83-9Downstream Products

29228-83-9Relevant articles and documents

A practical synthesis and spectroscopic study of new potentially biologically active S-lithocholic acid-substituted derivatives of 2-thiouracil

Pospieszny, Tomasz,Ma?ecka, Izabela,Paryzek, Zdzis?aw

, p. 4166 - 4169 (2010)

Five new S-3α-acetoxy-5β-lithocholic acid methyl ester-substituted derivatives of 2-thiouracil and 6-methyl-2-thiouracil have been prepared. 5-Morpholino-methyl-2-thiouracil, 5-piperidinomethyl-2- thiouracil, and 5-(4-methylpiperidino)methyl-2-thiouracil have been obtained via the Mannich reaction between 6-methyl-2-thiouracil, paraformaldehyde, and the cyclic secondary amines morpholine, piperidine, or 4-methylpiperidine in ethanol. The structures of the compounds were confirmed by spectral ( 1H NMR, 13C NMR, and FT-IR) analyses and mass spectrometry. Estimation of the pharmacotherapeutic potential has been accomplished for the synthesized compounds on the basis of Prediction of Activity Spectra for Substances (PASS).

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