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2,3-Naphthalenedicarboxylic acid, 1,2,3,4-tetrahydro-, cis- is a chemical compound with the molecular formula C12H12O4. It is a derivative of naphthalene, a hydrocarbon with two fused benzene rings, and features two carboxylic acid groups at the 2 and 3 positions. The compound is characterized by its cis-configuration, indicating that the two carboxylic acid groups are on the same side of the molecule. This specific arrangement of functional groups gives it unique chemical properties and reactivity compared to its trans-isomer. The compound is used in the synthesis of various pharmaceuticals, dyes, and other organic compounds due to its versatile chemical structure.

2305-27-3

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2305-27-3 Usage

Physical Appearance

White to off-white powder

Common Uses

Building block in the synthesis of pharmaceuticals and organic compounds
Chelating agent
Intermediate in dye and pigment production

Importance of cisIsomer

Significant in pharmaceutical synthesis due to specific stereochemical properties

Other Applications

Studied for potential use in organic electronic devices
Component in polymer materials

Check Digit Verification of cas no

The CAS Registry Mumber 2305-27-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,0 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2305-27:
(6*2)+(5*3)+(4*0)+(3*5)+(2*2)+(1*7)=53
53 % 10 = 3
So 2305-27-3 is a valid CAS Registry Number.

2305-27-3Downstream Products

2305-27-3Relevant academic research and scientific papers

Metallic Nickel Assisted Room-Temperature Generation and Diels-Alder Chemistry of o-Xylylene Intermediates

Inaba, Shin-ichi,Wehmeyer, Richard M.,Forkner, Matthew W.,Rieke, Reuben D.

, p. 339 - 344 (1988)

Highly reactive metallic nickel, prepared by the lithium metal reduction of nickel iodide using naphthalene as an electron carrier, was found to induce 1,4-dehalogenation of α,α'-dihalo-o-xylene derivatives at room temperature.The reaction proceeds in the presence of a variety of electron-deficient olefins, giving Diels-Alder cycloadducts in moderate to good yields presumably via the highly reactive intermediate o-xylylene 2. 1,3-Dibromoindan and 1,4-dibromo-1,2,3,4-tetrahydronaphthalene also react in the presence of electron-deficient olefins to give bridged cycloadducts in moderate yields.Methoxy as well as electron-deficient substituents such as bromide and nitrile groups on the aromatic ring of the starting dibromide were shown to be compatible with the reaction conditions yielding substituted cycloadducts in good yields.

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