Product Detail
Butyraldehyde-2-13C
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.
Butyraldehyde-2-13C Product Information
Butyraldehyde-2-13C 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-103612.
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
Butyraldehyde-2-13C
CAS No.
33683-08-8
CAT No.
CS-T-103612
Molecular Formula
C₃¹³CH₈O
Molecular Weight
73.1
Category
API Family
Storage Condition
Refer MSDS for complete information.
SMILES
CC[13CH2]C=O
IUPAC Name
Butyraldehyde-2-13C; Butal-2-13C; Butaldehyde-2-13C; Butanaldehyde-2-13C; Butyl Aldehyde-2-13C; Butyral-2-13C; Butyric Aldehyde-2-13C; Butyrylaldehyde-2-13C; NSC 62779-2-13C; n-Butanal-2-13C; n-Butyl Aldehyde-2-13C; n-Butyraldehyde-2-13C; n-Butyric Aldehyde-2-13C;
Hazard Compound
Refer MSDS for complete information.
Description
Overview
Butyraldehyde-2-13C is the labeled form of Butanal (B689890). Butanal is used as a reagent in the synthesis of N-substituted Oseltamivir (O701000) derivatives as potent and selective inhibitors of H5N1 influenza neuraminidase.
Synonyms
Butyraldehyde-2-13C; Butal-2-13C; Butaldehyde-2-13C; Butanaldehyde-2-13C; Butyl Aldehyde-2-13C; Butyral-2-13C; Butyric Aldehyde-2-13C; Butyrylaldehyde-2-13C; NSC 62779-2-13C; n-Butanal-2-13C; n-Butyl Aldehyde-2-13C; n-Butyraldehyde-2-13C; n-Butyric Aldehyde-2-13C;
Application Notes
Butyraldehyde-2-13C is the labeled form of Butanal (B689890). Butanal is used as a reagent in the synthesis of N-substituted Oseltamivir (O701000) derivatives as potent and selective inhibitors of H5N1 influenza neuraminidase.
References
Xie, Y., et al.: J. Med. Chem., 57, 8445 (2014)
