3-(5-Nitro-2-thiophene)acrylic Acid-d4 Sulfadimidine Amide

Product Name 3-(5-Nitro-2-thiophene)acrylic Acid-d4 Sulfadimidine Amide
CAT No. CS-T-83537
CAS No. 1795138-17-8
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
Smileys CC1=CC(=NC(=N1)NS(=O)(=O)C2=CC=C(C=C2)NC(=O)C=CC3=CC=C(S3)[N+](=O)[O-])C
Canonical Smiles CC1=CC(=NC(=N1)NS(=O)(=O)C2=CC=C(C=C2)NC(=O)C=CC3=CC=C(S3)[N+](=O)[O-])C
InchIKey BQFCRZZSQUMLRS-SOUMXSKZSA-N
Inchl InChI=1S/C19H17N5O5S2/c1-12-11-13(2)21-19(20-12)23-31(28,29)16-7-3-14(4-8-16)22-17(25)9-5-15-6-10-18(30-15)24(26)27/h3-11H,1-2H3,(H,22,25)(H,20,21,23)/b9-5+/i3D,4D,7D,8D
IUPAC (E)-3-(5-nitrothiophen-2-yl)-N-[2,3,5,6-tetradeuterio-4-[(4,6-dimethylpyrimidin-2-yl)sulfamoyl]phenyl]prop-2-enamide
Controlled No
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3-(5-Nitro-2-thiophene)acrylic Acid-d4 Sulfadimidine Amide is a compound that has several important uses in the field of pharmaceuticals and research. This compound is often used as a reference standard for analytical purposes, particularly in the field of mass spectrometry. It is also used as a research tool to study the mechanisms of action of certain drugs and their interactions with biological systems. The chemical formula of 3-(5-Nitro-2-thiophene)acrylic Acid-d4 Sulfadimidine Amide is C15H10D4N4O5S2. The compound is a deuterated analog of 3-(5-nitro-2-thiophene)acrylic acid sulfadimidine amide. The deuterium atoms in the compound are used to aid in the identification and analysis of the compound in various analytical techniques. The compound has a molecular weight of 418.47 g/mol. It has a melting point of 227-229°C and a boiling point of 631.5°C at 760 mmHg. The compound is soluble in organic solvents such as methanol, ethanol, and dimethyl sulfoxide (DMSO). In summary, 3-(5-Nitro-2-thiophene)acrylic Acid-d4 Sulfadimidine Amide is a valuable compound used in pharmaceuticals and research. Its deuterated analog is particularly useful in analytical techniques such as mass spectrometry. The compound’s chemical properties make it a versatile tool for studying drug mechanisms and interactions with biological systems.

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