13571-18-1 Usage
Uses
Used in Chemical Synthesis:
[2-(aminooxy)propyl]benzene hydrochloride (1:1) is used as a reagent in chemical synthesis for its ability to participate in various chemical reactions, contributing to the formation of different organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [2-(aminooxy)propyl]benzene hydrochloride (1:1) is used as an intermediate in the synthesis of various drugs, leveraging its reactive functional groups to create therapeutically relevant molecules.
Used in Research and Development:
[2-(aminooxy)propyl]benzene hydrochloride (1:1) is utilized as a research compound for exploring new chemical pathways and understanding the reactivity of the aminooxy propyl group in different reaction conditions.
It is crucial to handle [2-(aminooxy)propyl]benzene hydrochloride (1:1) with care and adhere to proper safety protocols due to its chemical nature and potential reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 13571-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,7 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13571-18:
(7*1)+(6*3)+(5*5)+(4*7)+(3*1)+(2*1)+(1*8)=91
91 % 10 = 1
So 13571-18-1 is a valid CAS Registry Number.
13571-18-1Relevant articles and documents
Donor–Acceptor Complex Enables Alkoxyl Radical Generation for Metal-Free C(sp3)–C(sp3) Cleavage and Allylation/Alkenylation
Zhang, Jing,Li, Yang,Xu, Ruoyu,Chen, Yiyun
, p. 12619 - 12623 (2017)
The alkoxyl radical is an essential and prevalent reactive intermediate for chemical and biological studies. Here we report the first donor–acceptor complex-enabled alkoxyl radical generation under metal-free reaction conditions induced by visible light. Hantzsch ester forms the key donor–acceptor complex with N-alkoxyl derivatives, which is elucidated by a series of spectrometry and mechanistic experiments. Selective C(sp3)-C(sp3) bond cleavage and allylation/alkenylation is demonstrated for the first time using this photocatalyst-free approach with linear primary, secondary, and tertiary alkoxyl radicals.
