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2-(ALLYLTHIO)-6-METHYLPYRIMIDIN-4-OL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62459-06-7

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62459-06-7 Usage

Molecular Structure

Pyrimidine derivative with an allylthio group and a methyl group

Potential Uses

Antiviral and anticancer agent, antioxidant, neuroprotective agent, and anti-inflammatory agent

Mechanism of Action

Inhibition of an enzyme involved in viral replication and tumor cell growth

Current Status

Ongoing research and development for potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 62459-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,5 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62459-06:
(7*6)+(6*2)+(5*4)+(4*5)+(3*9)+(2*0)+(1*6)=127
127 % 10 = 7
So 62459-06-7 is a valid CAS Registry Number.

62459-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-2-prop-2-enylsulfanyl-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 6-methyl-2-prop-2-enylthio-3-hydropyrimidin-4-one

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:62459-06-7 SDS

62459-06-7Downstream Products

62459-06-7Relevant academic research and scientific papers

Synthesis of 2-alkyl(aralkyl)sulfanyl-6-methylpyrimidin-4(3H)-ones and 4-alkyl(aralkyl)oxy-2-alkyl(aralkyl)sulfanyl-6-methylpyrimidines

Rakhimov,Titova

, p. 96 - 102 (2007/10/03)

2-Alkyl(aralkyl)sulfanyl-6-methylpyrimidin-4(3H)-ones and 4-alkyl(aralkyl)oxy-2-alkyl(aralkyl)-sulfanyl-6-methylpyrimidines having similar or different substituents on the sulfur and oxygen atoms were synthesized by alkylation of sodium salts derived from

Halocyclization of substituted 2-(alkenylthio)pyrimidin-6-ones

Slivka,Gevaza,Staninets

, p. 660 - 666 (2007/10/03)

Bromination and iodation of 2-(alkenylthio)pyrimidin-6-ones occur selectively and lead to formation of the corresponding 7-oxo-2,3- dihydrothiazolopyrimidinium or 8-oxo-3,4-dihydro-2H-pyrimidothiazinium salts. The selectivity of the reaction is controlled

IODOCYCLIZATION OF 2-ALLYLTHIO-4(3H)-PYRIMIDINONES

Kim, D. G.,Shmygarev, V. I.

, p. 183 - 185 (2007/10/03)

It has been established that the iodocyclization of 2-allylthio-4(3H)-pyrimidinones occurs at the N(1) nitrogen atom with the formation of 3-iodomethyl-7-oxo-2,3-dihydro-8H-thiazolopyrimidinium iodides and triiodides.

Palladium-Catalyzed Polyhetero-Claisen Rearrangement of 2-(Allylthio)pyrimidin-4(3H)-ones

Mizutani, Masato,Sanemitsu, Yuzuru,Tamaru, Yoshinao,Yoshida, Zen-ichi

, p. 764 - 768 (2007/10/02)

The regioselective S -> N allylic transposition of 2-(allylthio)pyrimidin-4(3H)-ones (3) has been performed by catalysis of Pd(II) salts.Generally the rearrangement gives the N-1 alkylation product predominantly over the N-3-alkylation product.Substituents at the 6-position of 3 reverse the selectivity.Both N-1 and N-3 rearrangement products were transformed to thiazolopyrimidones.

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