(4-Chlorobenzoylamino)malonic Acid-d4 Diethyl Ester

Product Name (4-Chlorobenzoylamino)malonic Acid-d4 Diethyl Ester
CAT No. CS-T-50594
CAS No. 1216553-23-9
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Canonical Smiles CCOC(=O)C(C(=O)OCC)NC(=O)C1=CC=C(C=C1)Cl
InchIKey KTKBMOLVXVIHQA-KDWZCNHSSA-N
Inchl InChI=1S/C14H16ClNO5/c1-3-20-13(18)11(14(19)21-4-2)16-12(17)9-5-7-10(15)8-6-9/h5-8,11H,3-4H2,1-2H3,(H,16,17)/i5D,6D,7D,8D
IUPAC diethyl 2-[(4-chloro-2,3,5,6-tetradeuteriobenzoyl)amino]propanedioate
Controlled No
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(4-Chlorobenzoylamino)malonic Acid-d4 Diethyl Ester is a deuterated organic compound that is used in various fields such as pharmaceuticals, chemical synthesis, and research. The compound is also known as (4-Chlorobenzoyl) amino-malonic acid-d4 diethyl ester and has a molecular formula of C15H11ClD4NO5. The compound is commonly used in chemical synthesis as a starting material for the synthesis of other organic compounds. Its unique deuterated form makes it useful in NMR spectroscopy, allowing for the identification and quantification of the compound and its products. Additionally, the compound has been used in the synthesis of potential antitumor agents, making it a valuable tool in pharmaceutical research. The chemical information of (4-Chlorobenzoylamino)malonic Acid-d4 Diethyl Ester indicates that it has a melting point of approximately 161-163°C and a boiling point of approximately 523.3°C at 760 mmHg. Its solubility in water is low, but it is soluble in organic solvents such as ethanol and methanol. The compound is considered to be relatively stable under normal conditions, but it may react with strong oxidizing agents and acids. Care should be taken when handling the compound, and appropriate safety measures should be followed. Overall, (4-Chlorobenzoylamino)malonic Acid-d4 Diethyl Ester is a useful tool in chemical synthesis and research, providing valuable information in the fields of pharmaceuticals and NMR spectroscopy.

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