6972-27-6

  • Product Name:6-Chloro-1,3-dimethyl-2,4-(1H,3H)-pyrimidinedione
  • Molecular Formula:C6H7ClN2O2
  • Purity:99%
  • Molecular Weight:174.587
Inquiry

Product Details

pd_meltingpoint:109-113 °C

Appearance:white or light white crystal powder

Factory Sells Best Quality 6-Chloro-1,3-dimethyl-2,4-(1H,3H)-pyrimidinedione 6972-27-6 with ISO standards

  • Molecular Formula:C6H7ClN2O2
  • Molecular Weight:174.587
  • Appearance/Colour:white or light white crystal powder 
  • Vapor Pressure:0.0906mmHg at 25°C 
  • Melting Point:109-113 °C 
  • Refractive Index:1.576 
  • Boiling Point:224.6 °C at 760 mmHg 
  • PKA:-3.53±0.40(Predicted) 
  • Flash Point:89.6 °C 
  • PSA:44.00000 
  • Density:1.43 g/cm3 
  • LogP:-0.26260 

6-Chloro-1,3-dimethyl-2,4-(1H,3H)-pyrimidinedione(Cas 6972-27-6) Usage

InChI:InChI=1/C6H7ClN2O2/c1-8-4(7)3-5(10)9(2)6(8)11/h3H,1-2H3

6972-27-6 Relevant articles

Doxofylline impurity and preparation method thereof

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Paragraph 0020-0024, (2019/05/22)

The invention provides a doxofylline imp...

Iodine/persulfate-promoted site-selective direct thiolation of quinolones and uracils

Beukeaw, Danupat,Noikham, Medena,Yotphan, Sirilata

supporting information, (2019/09/03)

A simple and general method for direct t...

Pd/PTABS: Catalyst for Room Temperature Amination of Heteroarenes

Murthy Bandaru, Siva Sankar,Bhilare, Shatrughn,Chrysochos, Nicolas,Gayakhe, Vijay,Trentin, Ivan,Schulzke, Carola,Kapdi, Anant R.

supporting information, p. 473 - 476 (2018/01/28)

A mild and highly efficient catalytic am...

A natural product four methyl uric acid fully synthetic method

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Paragraph 0033; 0034; 0035, (2017/08/25)

The invention relates to a total synthes...

6972-27-6 Process route

1,3-dimethylbarbituric acid
769-42-6

1,3-dimethylbarbituric acid

1,3-Dimethyl-6-chlorouracil
6972-27-6

1,3-Dimethyl-6-chlorouracil

Conditions
Conditions Yield
With water; trichlorophosphate; Heating;
93%
With water; trichlorophosphate; for 6h; Reflux; Large scale;
92.3%
With trichlorophosphate;
With trichlorophosphate; for 1h; Yield given; Heating;
With trichlorophosphate; for 2h; Heating;
With trichlorophosphate;
With trichlorophosphate; In water; at 22 - 26 ℃; Cooling; Reflux;
With trichlorophosphate; In water; for 3h; Cooling; Reflux;
With trichlorophosphate; In water; for 3h; Reflux;
With trichlorophosphate; In water; for 3h; Reflux; Large scale;
0.9 kg
With trichlorophosphate; In water; for 1h; Inert atmosphere; Reflux;
8 g
With trichlorophosphate; In water; at 0 - 90 ℃; for 2.5h;
20 g
6-chlorouracil
4270-27-3

6-chlorouracil

1,3-Dimethyl-6-chlorouracil
6972-27-6

1,3-Dimethyl-6-chlorouracil

Conditions
Conditions Yield
With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 70 ℃; for 3h;

6972-27-6 Upstream products

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    6320-15-6

    6-chloro-2,4-dimethoxypyrimidine

  • 74-88-4
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    methyl iodide

  • 769-42-6
    769-42-6

    1,3-dimethylbarbituric acid

  • 4270-27-3
    4270-27-3

    6-chlorouracil

6972-27-6 Downstream products

  • 5770-43-4
    5770-43-4

    6-ethylamino-1,3-dimethyl-1H-pyrimidine-2,4-dione

  • 5770-44-5
    5770-44-5

    6-(2-hydroxyethylamino)-1,3-dimethylpyrimidine-2,4(1H,3H)-dion

  • 13177-82-7
    13177-82-7

    1,3-dimethyl-6-dimethylaminouracil

  • 5770-46-7
    5770-46-7

    6-n-butylamino-1,3-dimethyluracil