DL-Valine N-carboxy anhydride, with the CAS number 2816-12-8, is a cyclic derivative of the amino acid valine. It is characterized by its anhydride functional group, which is formed by the condensation of the carboxylic acid group of valine. This compound is typically a white to off-white solid and is soluble in polar organic solvents. As a member of the class of amino acid anhydrides, it can be used in peptide synthesis and as a building block in polymer chemistry, particularly in the preparation of polyamides and other related materials. The anhydride form is reactive, allowing it to participate in various chemical reactions, including ring-opening polymerization. Its reactivity is influenced by the presence of the anhydride group, making it a useful intermediate in organic synthesis. Safety precautions should be taken when handling this compound, as it may be irritant to skin and mucous membranes. Overall, DL-Valine N-carboxy anhydride serves as an important compound in both academic research and industrial applications.

DL-Valine N-carboxy anhydride

2816-12-8: 2,5-Oxazolidinedione, 4-(1-methylethyl)-, 2,5-Oxazolidinedione, 4-isopropyl-, 4-(1-Methylethyl)-2,5-oxazolidinedione, 4-(Propan-2-Yl)-1,3-Oxazolidine-2,5-Dione, <span class="text-smallcaps">DL</span>-Valine N-carboxy anhydride, Valine, N-carboxy-, cyclic anhydride, DL-Valine N-carboxy anhydride, 4-Isopropyloxazolidine-2,5-dione

4-Isopropyloxazolidine-2,5-dione

4-Isopropyloxazolidine-2,5-dione is a monomer that inhibits proteinases. It is synthesized by treating trifluoroacetic acid with an epoxide, which is then reacted with the appropriate alcohol. 4-Isopropyloxazolidine-2,5-dione can be used in solid phase synthesis to produce homochiral products. The nmr spectra of 4-isopropyloxazolidine-2,5-dione show one set of peaks at a chemical shift of 7.8 ppm and another set at 8.0 ppm. The abiotic degradation of glutamate also produces this product as a major product (about 70%). The target cells for 4-isopropyloxazolidine-2,5-dione are primarily cancer cells and neurons. In cancer cells it has shown an enhancement effect on the cytotoxic activity of enantiomer 1 when applied in combination

CAS 2816-12-8: DL-Valine N-carboxy anhydride

4-Isopropyloxazolidine-2,5-dione

Ref: 54-OR964676

4-Isopropyloxazolidine-2,5-dione

Ref: IN-DA003LLM

4-Isopropyloxazolidine-2,5-dione

Ref: 10-F447117

4-Isopropyloxazolidine-2,5-dione

Ref: 3D-CAA81612