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1-benzyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1208-14-6

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1208-14-6 Usage

Type of compound

Heterocyclic compound
Contains a ring structure with at least one ring atom being non-carbon (in this case, nitrogen and sulfur).
3. Derivative of pyrimidine family
A modified version of a pyrimidine compound, which is a type of organic compound with a six-membered ring structure and two nitrogen atoms.
4. Potential pharmaceutical and medicinal applications
The compound has been studied for its possible use in the development of new drugs due to its various pharmacological properties.
5. Potential antiviral properties
The compound may exhibit the ability to inhibit or destroy viruses, which could be useful in the treatment of viral infections.
6. Potential antitumor properties
The compound may have the ability to inhibit or prevent the growth and spread of cancer cells.
7. Potential antimicrobial properties
The compound may exhibit the ability to kill or inhibit the growth of microorganisms, such as bacteria and fungi.
8. Potential anti-inflammatory properties
The compound may help to reduce inflammation, which is a response to injury or infection in the body.
9. Potential analgesic properties
The compound may have the ability to relieve pain, making it a potential candidate for pain management applications.
10. Applications in drug discovery and development
Due to its range of potential pharmacological properties, 1-benzyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one is a promising candidate for further research and development in the field of pharmaceuticals and medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 1208-14-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1208-14:
(6*1)+(5*2)+(4*0)+(3*8)+(2*1)+(1*4)=46
46 % 10 = 6
So 1208-14-6 is a valid CAS Registry Number.

1208-14-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-2-sulfanylidenepyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 1-Benzyl-2-thioxo-2,3-dihydro-4(1H)-pyrimidinone

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:1208-14-6 SDS

1208-14-6Downstream Products

1208-14-6Relevant academic research and scientific papers

Solid-phase synthesis of 4(1H)-quinolone and pyrimidine derivatives based on a new scaffold - Polymer-bound cyclic malonic acid ester

Huang, Xian,Liu, Zhanxiang

, p. 6731 - 6737 (2002)

An efficient method for the preparation of polymer-bound cyclic malonic acid ester starting from Merrifield resin has been developed. Reaction of the resin-bound cyclic malonic acid ester with triethyl orthoformate and subsequent double substitution with

Straightforward pyrimidine ring construction: A versatile tool for the synthesis of nucleobase and nucleoside analogues

Robin, Aelig,Julienne, Karine,Meslin, Jean-Claude,Deniaud, David

, p. 634 - 643 (2007/10/03)

A general route to 1,2,4-trisubstituted pyrimidines is described in one to three steps from a common key precursor, diazadienium iodide 2. An efficient preliminary [4+2] cyclocondensation reaction between the azabutadiene building block 2 and various iso(thio)cyanates constitutes an original construction of the pyrimidine skeleton. Subsequent structural modifications on the heterocycle allow the elaboration of a 1-substituted pyrimidine library that includes nucleoside analogues. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

Improved One-Step Procedure for the Preparation of 1-Substituted and 1,3-Disubstituted Uracils and 2-Thiouracils

Winckelmann, Ib,Larsen, Erik H.

, p. 1041 - 1044 (2007/10/02)

A convenient one-pot procedure for the synthesis of 1-substituted and 1,3-disubstituted uracils and 2-thiouracils consists of acylation of ureas or thioureas with methyl 3,3-dimethoxypropanoate in the presence of a strong base, and acidic work-up.The yields range from 36 to 99percent.In all cases, only one regioisomer is isolated.

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