59173-62-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
1-Butanol, 2-amino-, hydrochloride is derived from 2-amino-1-butanol, a primary amine with a four-carbon chain, by forming a salt with hydrochloric acid.
Explanation
The compound contains a primary amine functional group, which is an amino group (-NH2) attached to the first carbon of the four-carbon chain.
Explanation
The hydrochloride salt form of 1-Butanol, 2-aminois used to improve its solubility in water and increase its stability for various applications.
Explanation
1-Butanol, 2-amino-, hydrochloride is utilized as a reagent or intermediate in various chemical and pharmaceutical processes.
Explanation
The compound serves as a precursor in the synthesis of pharmaceutical drugs, contributing to the development of new medications.
Explanation
1-Butanol, 2-amino-, hydrochloride can be used as a building block in the production of other organic compounds, expanding its utility in the chemical industry.
Structure
Hydrochloride salt of 2-amino-1-butanol
Primary amine
2-amino-1-butanol
Hydrochloride salt
Enhanced solubility and stability
Applications
Chemical and pharmaceutical processes
Precursor in drug synthesis
Pharmaceutical drug production
Building block
Production of other organic compounds
Check Digit Verification of cas no
The CAS Registry Mumber 59173-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,7 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59173-62:
(7*5)+(6*9)+(5*1)+(4*7)+(3*3)+(2*6)+(1*2)=145
145 % 10 = 5
So 59173-62-5 is a valid CAS Registry Number.
59173-62-5Relevant articles and documents
Radical-mediated intramolecular β-C(sp3)-H amidation of alkylimidates: Facile synthesis of 1,2-amino alcohols
Mou, Xue-Qing,Chen, Xiang-Yu,Chen, Gong,He, Gang
supporting information, p. 515 - 518 (2018/01/19)
A new radical-mediated intramolecular β-C(sp3)-H amidation reaction of O-alkyl trichloro- or arylimidates is reported. Various oxazolines were efficiently prepared from easily accessible alcohol starting materials. The trichloro-oxazoline products can be hydrolyzed under mild conditions to give valuable 1,2-amino alcohols. This amidation reaction exhibits a broad substrate scope and good functional group tolerance, and offers a powerful means for the C(sp3)-H functionalization of alcohols. Mechanistic studies suggest that a sequence of 1,5-HAT of an imidate radical, iodination and cyclization might be operative.
