141-90-2

  • Product Name:2-Thiouracil
  • Molecular Formula:C4H4N2OS
  • Purity:99%
  • Molecular Weight:
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Product Details

Appearance:white to cream fine crystalline powder

2-Thiouracil 141-90-2 manufacturer, in stock, low price

  • Molecular Formula:C4H4N2OS
  • Molecular Weight:128.155
  • Appearance/Colour:white to cream fine crystalline powder 
  • Vapor Pressure:5.45E-05mmHg at 25°C 
  • Melting Point:>300 °C(lit.) 
  • Refractive Index:1.677 
  • Boiling Point:337.2 °C at 760 mmHg 
  • PKA:pKa 7.46 (Uncertain) 
  • Flash Point:157.7 °C 
  • PSA:80.74000 
  • Density:1.46 g/cm3 
  • LogP:0.43250 

2-Thiouracil 141-90-2 Usage

2-Thiouracil is white to cream fine crystalline powder. It acts as an anticancer, antithyroid, and antiviral agent. 2-Thiouracil is a substance with effective biological and pharmacological activities, which has been used in the synthesis and characterization of silver colloid and film substrates and their applications in surface-enhanced Raman scattering (SERS). 

Definition

ChEBI: A nucleobase analogue that is uracil in which the oxo group at C-2 is replaced by a thioxo group.

Purification Methods

Crystallise 2-thiouracil from water or EtOH. 

InChI:InChI=1/C4H4N2OS/c7-3-1-2-5-4(8)6-3/h1-2H,(H2,5,6,7,8)

141-90-2 Relevant articles

A simple strategy to enhance the luminescence of metal nanoclusters and its application for turn-on detection of 2-thiouracil and hyaluronidase

Miao Liang , Zhongli Lei , Yiling Li, Yan Xiao

Talanta Volume 236, 1 January 2022, 122876

Since 2-thiouracil (2-TU), a common anticancer, antithyroid, and antiviral agent, featured a similar molecular structure of ATT, this luminescence enhancement strategy can be designed to sensitive and selective turn-on detect 2-TU.

Kinetics and adsorption isotherm model of 2-thiouracil adsorbed onto the surface of reduced graphene oxide-copper oxide nanocomposite material

Pramanand Kumar, Subrata Das

Journal of Molecular Structure Volume 1268, 15 November 2022, 133723

We report the synthesis of rGO-CuO using the chemical modification method, characterization, and the adsorption isotherm behavior of the nanocomposite material for the removal of 6-amino-2-thiouracil (6A2TU) and 6-amino-5-nitroso-2-thiouracil (6A5NTU) in an aqueous medium.

141-90-2 Process route

ethyl 3-(N-methylcyanamino)-2-butenoate
75039-91-7

ethyl 3-(N-methylcyanamino)-2-butenoate

2-thiouracil
141-90-2,156-82-1

2-thiouracil

1-(methyl)-thiourea
598-52-7

1-(methyl)-thiourea

1,6-dimethyl-2-thiouracil
33238-58-3

1,6-dimethyl-2-thiouracil

Conditions
Conditions Yield
With hydrogen sulfide; In ethanol; at 30 - 40 ℃;
0.2 g
0.2 g
0.5 g
2-thiocytidine
13233-20-0,13239-97-9

2-thiocytidine

2-thiouracil
141-90-2,156-82-1

2-thiouracil

2-thiocytosine
333-49-3

2-thiocytosine

2-thiouridine
20235-78-3

2-thiouridine

Conditions
Conditions Yield
With formic acid; water; at 60 ℃; for 1296h; pH=3;
38%
34%
18%

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