1533519-92-4 Usage
General Description
4-cyclopropylnaphthalen-1-amine hydrochloride is a chemical compound with the molecular formula C13H13ClN. It is a derivative of cyclopropylamine and is commonly used as a building block in organic synthesis. 4-cyclopropylnaphthalen-1-aMine hydrochloride is a white to off-white solid, and it is soluble in water, methanol, and ethanol. It has been used as a reactant in the synthesis of various pharmaceutical and agrochemical compounds. 4-cyclopropylnaphthalen-1-amine hydrochloride is also known for its potential biological activity and has been studied for its antimicrobial and anticancer properties. 4-cyclopropylnaphthalen-1-aMine hydrochloride should be handled and used in accordance with proper safety protocols and regulations.
Check Digit Verification of cas no
The CAS Registry Mumber 1533519-92-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,3,3,5,1 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1533519-92:
(9*1)+(8*5)+(7*3)+(6*3)+(5*5)+(4*1)+(3*9)+(2*9)+(1*2)=164
164 % 10 = 4
So 1533519-92-4 is a valid CAS Registry Number.
1533519-92-4Relevant articles and documents
Compound, preparation method and applications thereof
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Paragraph 0089-0090, (2020/03/25)
The invention provides an N-(4-cyclopropylnaphthyl)-formamide compound represented by a structural formula I, and a preparation method thereof, wherein R is defined in the specification. The inventionalso provides a preparation method of 4-cyclopropyl-1-naphthylamine, wherein the preparation method comprises: hydrolyzing the compound represented by the structural formula I in the presence of an alkali or an acid to obtain the 4-cyclopropyl-1-naphthylamine. The invention also provides a lesinurad preparation method, which comprises the following steps: preparing 4-cyclopropyl-1-naphthylamine from the compound represented by the structural formula I, and preparing Lesinurad according to the known synthetic route in the field.