CAS 5466-93-3
:diethyl benzene-1,4-diylbiscarbamate
Description:
Diethyl benzene-1,4-diylbiscarbamate, with the CAS number 5466-93-3, is an organic compound characterized by its structure, which features two carbamate functional groups attached to a benzene ring. This compound is typically a white to off-white solid and is soluble in organic solvents, but its solubility in water is limited. It is known for its applications in various fields, including as a potential intermediate in organic synthesis and in the development of agrochemicals. The presence of the carbamate groups imparts specific reactivity, making it useful in forming derivatives or in polymer chemistry. Additionally, diethyl benzene-1,4-diylbiscarbamate may exhibit biological activity, which necessitates careful handling and consideration of safety protocols during its use. As with many organic compounds, it is important to assess its stability, reactivity, and potential environmental impact. Proper storage conditions and safety measures should be observed to mitigate any risks associated with its handling.
Formula:C12H16N2O4
InChI:InChI=1/C12H16N2O4/c1-3-17-11(15)13-9-5-7-10(8-6-9)14-12(16)18-4-2/h5-8H,3-4H2,1-2H3,(H,13,15)(H,14,16)
SMILES:CCOC(=O)Nc1ccc(cc1)NC(=O)OCC
Synonyms:- carbamic acid, N,N'-1,4-phenylenebis-, diethyl ester
- Diethyl 1,4-phenylenebiscarbamate
- 1,4-Bis(ethoxycarbonylamino)benzene
- Rivaroxaban Impurity 136
- Carbamic acid, N,N'-1,4-phenylenebis-, C,C'-diethyl ester
- N-[4-(Ethoxycarbonylamino)phenyl]carbamic acid ethyl ester
- ethyl N-[4-(ethoxycarbonylamino)phenyl]carbamate
- 1,4-Phenylenebis(carbamic acid ethyl) ester
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