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1020414-33-8

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  • Cas no.1020414-33-8 98% 1-NaphthaleneMethanaMine, 7,8-dihydro-伪-Methyl-N-[3-[3-(trifluoroMethyl)phenyl]propyl]-, hydrochloride (1:1), (伪R)-

    Cas No: 1020414-33-8

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1020414-33-8 Usage

General Description

1-Naphthalenemethanamine, 7,8-dihydro-α-methyl-N-[3-[3-(trifluoromethyl)phenyl]propyl]-, hydrochloride (1:1), (αR)- is a chemical compound that is commonly referred to as naphazoline hydrochloride. It is a nasal decongestant and vasoconstrictor that is used to relieve nasal congestion caused by allergies, sinusitis, and the common cold. Naphazoline hydrochloride works by constricting blood vessels in the nasal passages, which reduces swelling and congestion. It is typically available in over-the-counter nasal sprays and eye drops, and should be used as directed by a healthcare professional due to potential side effects and drug interactions.

Check Digit Verification of cas no

The CAS Registry Mumber 1020414-33-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,4,1 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1020414-33:
(9*1)+(8*0)+(7*2)+(6*0)+(5*4)+(4*1)+(3*4)+(2*3)+(1*3)=68
68 % 10 = 8
So 1020414-33-8 is a valid CAS Registry Number.

1020414-33-8Upstream product

1020414-33-8Downstream Products

1020414-33-8Relevant articles and documents

Dihydronaphthalene compounds, compositions, uses thereof, and methods for synthesis

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Page/Page column 52-53; figure 1, (2008/06/13)

The present invention relates to novel dihydronaphthalene compounds, compositions, methods for using the same, and processes for preparing the same. The present invention also relates to novel total synthesis approaches for preparing these compounds. In addition, the present invention relates to methods of producing quantities of isomers of these compounds and separating and purifying them using chiral separation techniques. The present invention also relates to methods of producing quantities of a single isometric compound without the need for chiral separation techniques.

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