5-Methylfurfural-d3

Stable Isotope Reagent API Family: . CAT No. CS-T-103733 CAS No. 620-02-0(unlabelled)
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Product Detail

5-Methylfurfural-d3

. Stable Isotope Reagent
Stock Status: Enquire
Live
For Research & Analytical Purposes. Not for Personal use.
Category Stable Isotope Reagent
API Family .
Storage Refer MSDS for complete information.
Hazard Information Refer MSDS for complete information.

5-Methylfurfural-d3 Product Information

5-Methylfurfural-d3 is listed under Stable Isotope Reagent. It is associated with . and is intended for analytical research, quality control and pharmaceutical reference standard applications. The product is supplied by Clearsynth under CAT No. CS-T-103733.

Clearsynth provides this compound for research and analytical use, with product information including CAS number, molecular formula, molecular weight, stock enquiry details and supporting documentation.

Technical Data

Product Name
5-Methylfurfural-d3
CAS No.
620-02-0(unlabelled)
CAT No.
CS-T-103733
Molecular Formula
C₇H₅D₃O
Molecular Weight
111.16
API Family
Storage Condition
Refer MSDS for complete information.
SMILES
O=CC(O1)=CC=C1C([2H])([2H])[2H]
IUPAC Name
Deuterated 5-Methylfurfural
Hazard Compound
Refer MSDS for complete information.

Description

Overview
5-Methylfurfural-d3 is an isotopic labeled compound of 5-Methylfurfural (M305470). 5-Methylfurfural is a common chemical reagent used in a wide variety of chemical reactions and organic synthesis. Polycyclic pyridazine based derivatives are synthesized with this compound to form antimicrobial agents. Also used in the preparation of antiinflammatory diarylpentanoid analogues.
Synonyms
Deuterated 5-Methylfurfural
Application Notes
5-Methylfurfural-d3 is an isotopic labeled compound of 5-Methylfurfural (M305470). 5-Methylfurfural is a common chemical reagent used in a wide variety of chemical reactions and organic synthesis. Polycyclic pyridazine based derivatives are synthesized with this compound to form antimicrobial agents. Also used in the preparation of antiinflammatory diarylpentanoid analogues.
References
Deeb, A. et al.: Eur. Chem. Bull., 3, 897 (2014); Leong, S. et al.: Molecules, 19, 16058 (2014);
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