• Chemical Name 1-propyl-3-(p-tolylsulphonyl)urea
  • CAS No. 24570-88-5
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Quality Manufacturer Supply High Purity 99% 1-propyl-3-(p-tolylsulphonyl)urea 24570-88-5 with Reasonable Price

  • Molecular Formula: C11H16 N2 O3 S
  • Molecular Weight: 256.326
  • Melting Point: 151-152 °C 
  • PKA: 5.26±0.10(Predicted) 
  • PSA: 87.14000 
  • Density: 1.21g/cm3 
  • LogP: 3.06900 

1-propyl-3-(p-tolylsulphonyl)urea(Cas 24570-88-5) Usage

Mechanism of action

Inhibits thyroperoxidase PTU works by inhibiting the enzyme thyroperoxidase, which is necessary for the production of thyroid hormone, thus preventing excessive hormone production.

Form and administration

Tablet form, taken orally PTU is available as a medication in tablet form and is typically taken orally by patients.

Precautions

Use under doctor's guidance, potential side effects and interactions It is important to use PTU under the guidance of a doctor, as it can have serious side effects and interactions with other medications.

General Description

1-propyl-3-(p-tolylsulphonyl)urea is a chemical compound with the molecular formula C11H16N2O3S. It is also known as PTU or 6-propyl-2-thiouracil and is used in medicine to treat hyperthyroidism. PTU works by preventing the thyroid gland from producing excessive amounts of thyroid hormone. It accomplishes this by inhibiting the enzyme thyroperoxidase, which is necessary for the production of thyroid hormone. PTU is available as a medication in tablet form and is typically taken orally. It is important to use PTU under the guidance of a doctor, as it can have serious side effects and interactions with other medications.

InChI:InChI=1/C11H16N2O3S/c1-3-8-12-11(14)13-17(15,16)10-6-4-9(2)5-7-10/h4-7H,3,8H2,1-2H3,(H2,12,13,14)

24570-88-5 Relevant articles

A facile synthesis of sulfonylureas: Via water assisted preparation of carbamates

Tanwar, Dinesh Kumar,Ratan, Anjali,Gill, Manjinder Singh

, p. 4992 - 4999 (2017/07/11)

A novel and simple approach to the synth...

Design and development of sulfonylurea derivatives as zinc metalloenzyme modulators

Hadianawala, Murtuza,Datta, Bhaskar

, p. 8923 - 8929 (2016/02/05)

Sulfonamide derivatives are an important...

Mechanosynthesis of pharmaceutically relevant sulfonyl-(thio)ureas

Tan, Davin,?trukil, Vjekoslav,Mottillo, Cristina,Fri??i?, Tomislav

supporting information, p. 5248 - 5250 (2014/05/06)

We demonstrate the first application of ...

Lewis Acid Catalysed Preparation of some Carbamates and Sulphonylureas. Application to the Determination of Enantiomeric Purity of Chiral Alcohols

Irie, Hiroshi,Nishimura, Masataka,Yoshida, Morihiro,Ibuka, Toshiro

, p. 1209 - 1210 (2007/10/02)

Lewis acids such as boron trifluoride-di...

24570-88-5 Process route

Propyl isocyanate
110-78-1

Propyl isocyanate

toluene-4-sulfonamide
70-55-3

toluene-4-sulfonamide

4-methyl-N-( propylcarbamoyl)benzenesulfonamide
24570-88-5

4-methyl-N-( propylcarbamoyl)benzenesulfonamide

Conditions
Conditions Yield
With copper(l) chloride; In nitromethane; at 20 ℃; for 2h; Milling;
86%
With boron trifluoride diethyl etherate; In diethyl ether; Ambient temperature;
68%
With sodium hydroxide;
propylamine
107-10-8,42939-71-9

propylamine

sodium isocyanate
917-61-3

sodium isocyanate

p-toluenesulfonyl chloride
98-59-9

p-toluenesulfonyl chloride

4-methyl-N-( propylcarbamoyl)benzenesulfonamide
24570-88-5

4-methyl-N-( propylcarbamoyl)benzenesulfonamide

Conditions
Conditions Yield
With pyridine; In acetonitrile; at 20 ℃; for 5h;
53%

24570-88-5 Upstream products

  • 51506-31-1
    51506-31-1

    N-(allylcarbamoyl)-4-methylbenzenesulfonamide

  • 110-78-1
    110-78-1

    Propyl isocyanate

  • 70-55-3
    70-55-3

    toluene-4-sulfonamide

  • 623-95-0
    623-95-0

    1,3-dipropylurea

24570-88-5 Downstream products

  • 1888-33-1
    1888-33-1

    N-acetyl-(4-methylbenzene)sulfonamide