1-Methyl-5-nitro-1H-benzimidazole-2-butanoic Acid Ethyl Ester-d3

Product Name 1-Methyl-5-nitro-1H-benzimidazole-2-butanoic Acid Ethyl Ester-d3
CAT No. CS-T-58448
CAS No. 3543-72-4(Unlabeled)
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
Therapeutic Anti-Cancer / Oncology
Smileys [O-][N+](C1=CC=C2N(C(CCCC(OCC)=O)=NC2=C1)C([2H])([2H])[2H])=O
Canonical Smiles CCOC(=O)CCCC1=NC2=C(N1C)C=CC(=C2)[N+](=O)[O-]
InchIKey VJVBGSJZBDBEIF-UHFFFAOYSA-N
Inchl InChI=1S/C14H17N3O4/c1-3-21-14(18)6-4-5-13-15-11-9-10(17(19)20)7-8-12(11)16(13)2/h7-9H,3-6H2,1-2H3
IUPAC ethyl 4-(1-methyl-5-nitrobenzimidazol-2-yl)butanoate
Controlled No
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1-Methyl-5-nitro-1H-benzimidazole-2-butanoic Acid Ethyl Ester-d3 is a deuterated derivative of the organic compound 1-Methyl-5-nitro-1H-benzimidazole-2-butanoic Acid Ethyl Ester. This compound is a synthetic organic intermediate used in the production of various pharmaceuticals, agrochemicals, and other fine chemicals. The compound features a benzimidazole ring system with a nitro group at position 5 and a methyl group at position 1. The butanoic acid ethyl ester functional group is attached to the nitrogen atom of the benzimidazole ring. The deuterium atoms in the compound are useful for studying the metabolism and biotransformation of the parent compound in biological systems. The compound is typically used in small quantities as a reactant in chemical synthesis, where it undergoes various chemical transformations to produce the desired end product. It can also be used as a reference standard in analytical chemistry for the detection and quantification of the parent compound in various samples. In terms of safety, the compound is considered hazardous and must be handled with caution. It is recommended to wear appropriate personal protective equipment when working with this compound and to follow proper handling and disposal procedures.

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