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1,3-Dimethylbarbituric acid / 250 G

Purity: 99.0% (T)
Synonym: N,N'-Dimethylbarbituric acid; 1,3-dimethyl-1,3-diazinane-2,4,6-trione; 1,3-Dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione
Molecular Formula: C6H8N2O3
Molecular Weight: 156.14
SKU: MND-43317
CAS Number: 769-42-6
MDL number: MFCD00006675
EC Number: 212-211-7
Form: solid
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 250 G  
121.80 EUR



Safety Information


Hazard Statements

H302
H318

Precautionary Statements

P280
P264
P270
P301 + P312
P501
P305 + P351 + P338

Pictograms



Properties

Signal WordDanger
Flash Point (C)Not available
Flash Point (F)Not available
Melting Point121-123 °C (lit.);123-126 °C;

 Product Description

1,3-DIMETHYLBARBITURIC ACID is a chemical compound commonly utilized as a precursor in the synthesis of pharmaceuticals and herbicides. It is characterized by its barbiturate structure and is known for its role in organic synthesis.

 

Application:

1,3-DIMETHYLBARBITURIC ACID finds application as a key intermediate in the production of barbiturate-based pharmaceuticals and herbicides. It is utilized in organic synthesis processes to create compounds with sedative and herbicidal properties.

 

 

Articles:

- Metal-ligand cooperative iridium complex catalyzed C-alkylation of oxindole and 1,3-dimethylbarbituric acid using alcohols

Publication Date: Available online 16 July 2022

Ao Song, Yunbo Liu, Xuan Jin, Dianrun Su, Zhaopeng Li, Shengsheng Yu, Lingbao Xing, Xiangchao Xu, Rongzhou Wang, Feng Li

https://doi.org/10.1016/j.gresc.2022.07.002

 

- Reactions of 5-dihydrocotarnyl-1,3-dimethylbarbituric acid and other cotarnine derivatives with 1,3-dimethylbarbituric acid. X-ray diffraction analysis of a 5,5-spiro derivative of 1,3-dimethylbarbituric acid

Publication Date: August 2002

K. A. Krasnov, V. G. Kartsev & V. N. Khrustalev

https://doi.org/10.1023/A:1020983527851

 

- Synthesis, Structure and Reactions of 1,3-Dimethyl-5-bis(thiomethyl)methylenebarbituric Acid

Publication Date: June 2, 2014

Kamal Sweidan EMAIL logo , Ahmed Abu-Rayyan , Ahmad Al-Sheikh , Cäcilia Maichle-Mößmer , Manfred Steimann and Norbert Kuhn

https://doi.org/10.1515/znb-2009-0114