Product Detail
Pyrrolidine-2,2,5,5-d4 Hydrochloride
Stable Isotopes
Stock Status: Enquire
Live
For Research & Analytical Purposes. Not for Personal use.
Category
Stable Isotopes
API Family
--
Storage
Refer MSDS for complete information.
Hazard Information
Refer MSDS for complete information.
Pyrrolidine-2,2,5,5-d4 Hydrochloride Product Information
Pyrrolidine-2,2,5,5-d4 Hydrochloride is listed under Stable Isotopes. 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-102096.
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
Pyrrolidine-2,2,5,5-d4 Hydrochloride
CAS No.
-
CAT No.
CS-T-102096
Molecular Formula
C4H6D4ClN
Molecular Weight
111.61
Category
Storage Condition
Refer MSDS for complete information.
IUPAC Name
"Pyrrolidine-2,2,5,5-d4 Hydrochloride"
Hazard Compound
Refer MSDS for complete information.
Description
Overview
"Pyrrolidine-2,2,5,5-d4 Hydrochloride is the salt, labeled analogue of Pyrrolidine (P997950), a heterocyclic compound used as a building block in the synthesis of wide range of pharmaceutical compounds, namely matrix metalloprotein inhibitors (MMPIs) and aminopeptidase N inhibitors (APNIs)."
Synonyms
Pyrrolidine-d4 Hydrochloride; Azacyclopentane-d4 Hydrochloride; Azolidine-d4 Hydrochloride; Butylenimine-d4 Hydrochloride; NSC 62781-d4 Hydrochloride; Perhydropyrrole-d4 Hydrochloride; Prolamine-d4 Hydrochloride; Tetrahydropyrrolee-d4 Hydrochloride; Tetra
Application Notes
"Pyrrolidine-2,2,5,5-d4 Hydrochloride is the salt, labeled analogue of Pyrrolidine (P997950), a heterocyclic compound used as a building block in the synthesis of wide range of pharmaceutical compounds, namely matrix metalloprotein inhibitors (MMPIs) and aminopeptidase N inhibitors (APNIs)."
References
"Li, X. et al.: Mini-Rev. Med. Chem., 10, 794 (2010); Gragutan, I. et al.: Beil. J. Org. Chem., 7, 699 (2011)"