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4-(2-methoxynaphthalen-1-yl)-4-oxobutanoic acid is a complex organic compound with the molecular formula C15H14O5. It is characterized by a naphthalene ring, which is a fused ring system consisting of two benzene rings, with a methoxy group (-OCH3) attached to the second carbon. The compound also features a butanoic acid chain, which is a four-carbon aliphatic chain with a carboxyl group (-COOH) at the end. The butanoic acid chain is connected to the naphthalene ring through a carbonyl group (C=O), and it also contains an additional carbonyl group, making it a 4-oxobutanoic acid. This chemical structure gives the compound unique properties and potential applications in various fields, such as pharmaceuticals or chemical research.

81792-86-1

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81792-86-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81792-86-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,7,9 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 81792-86:
(7*8)+(6*1)+(5*7)+(4*9)+(3*2)+(2*8)+(1*6)=161
161 % 10 = 1
So 81792-86-1 is a valid CAS Registry Number.

81792-86-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2-methoxynaphthalen-1-yl)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:81792-86-1 SDS

81792-86-1Relevant academic research and scientific papers

Synthesis of functionalized molecular motors

Ter Wiel, Matthijs K. J.,Feringa, Ben L.

, p. 1789 - 1796 (2007/10/03)

Synthetic routes to two molecular motors are reported. The sterically hindered central olefinic bond connecting the two halves of these C 2-symmetric molecules was prepared by a McMurry reaction. In this way, a motor with two five-membered rings and a motor with two six-membered rings were prepared, both with two versatile methoxy substituents at positions not interfering with the rotary behavior. Georg Thieme Verlag Stuttgart.

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