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5-Pyrimidinecarbonitrile, 2-amino-1,4-dihydro-6-(methylthio)-4-thioxo-, monosodium salt is a complex organic compound with the chemical formula C6H6N3NaOS2. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound consisting of a six-membered ring with four carbon atoms and two nitrogen atoms. This specific compound features an amino group at the 2-position, a methylthio group at the 6-position, and a carbonitrile group at the 5-position. The 4-thioxo group indicates the presence of a sulfur atom double-bonded to an oxygen atom, forming a thione group. The monosodium salt form implies that one of the hydrogen atoms has been replaced by a sodium ion, making it a water-soluble salt. 5-Pyrimidinecarbonitrile, 2-amino-1,4-dihydro-6-(methylthio)-4-thioxo-, monosodium salt has potential applications in pharmaceuticals and chemical research, particularly in the synthesis of various biologically active molecules.

114460-75-2

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114460-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114460-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,4,6 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114460-75:
(8*1)+(7*1)+(6*4)+(5*4)+(4*6)+(3*0)+(2*7)+(1*5)=102
102 % 10 = 2
So 114460-75-2 is a valid CAS Registry Number.

114460-75-2SDS

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 sodium 2-amino-4-methylthio-5-cyanopyrimidine-6-thiolate

1.2 Other means of identification

Product number -
Other names sodium 2-amino-5-cyano-6-methylsulfanyl-pyrimidine-4-thiolate

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:114460-75-2 SDS

114460-75-2Downstream Products

114460-75-2Relevant academic research and scientific papers

Nucleic acid components and their analogs: Design and synthesis of novel cytosine thioglycoside analogs

Elgemeie, Galal H.,Salah, Ali M.,Abbas, Nermeen S.,Hussein, Hoda A.,Mohamed, Reham A.

, p. 139 - 150 (2017)

The synthesis of a new category of novel cytosine 4-thioglycoside analogs has been first accomplished. The main step of this strategy is the synthesis of sodium pyrimidine-4-thiolate through the condensation of 2-cyano-N-arylacetamides with sodium cyanocarbonimidodithioate, followed by coupling with α-bromo-sugars to afford the corresponding cytosine 4-thioglycoside analogs. The free thioglycosides were also prepared. Subsequent studies on the application of this strategy for the preparation of other potent pyrimidine thioglycosides are reported.

CYCLIZATION REACTION OF NITRILES. 26. SYNTHESIS, STRUCTURE, AND PROPERTIES OF 2-AMINO-4-METHYLTHIO-5-CYANO-6(1H)-PYRIMIDINETHIONE

Sharanin, Yu. A.,Shestopalov, A. M.,Nesterov, V. N.,Litvinov, V. P.,Mortikov, V. Yu.,et. al.

, p. 1105 - 1112 (2007/10/02)

2-Amino-4-methylthio-5-cyano-6(1H)-pyrimidinethione has been prepared via treatment of N-cyanodimethyldithioimidate or 1,1-di(methylthio)-2-thiocarbamoyl-2-cyanoethylene with cyanothioacetamide or cyanamide.The structure of the complex formed between 2-amino-4-methylthio-5-cyano-6(1H)-pyrimidinethione and urea has been studied by x-ray structural analysis.Thienopyrimidines and thiazolopyrimidinium salts have been synthesized based on the 6(1H)-pyrimidinethione.

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