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1H-Indene, 5,5'-(1,3-propanediyl)bis[2,3-dihydro- is a complex organic compound with the molecular formula C17H20. It is a derivative of indene, which is a tricyclic aromatic hydrocarbon. The compound features two 1H-inden-2,3-dihydro-5-yl groups connected by a 1,3-propanediyl bridge, resulting in a symmetrical structure. This chemical is primarily used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique molecular structure and reactivity. Its properties, such as stability and solubility, make it a valuable intermediate in organic synthesis, particularly in the preparation of more complex molecules with potential applications in various industries.

1785-55-3

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1785-55-3 Usage

Type of compound

Indene derivative

Structure

1,3-propanediyl bridge connecting two 2,3-dihydroindene moieties

Uses

Production of pharmaceuticals, agrochemicals, and as a chemical intermediate in the synthesis of other organic compounds

Potential properties

Biological and pharmacological properties

Variations

Specific chemical and physical properties, uses, and applications may vary depending on the specific isomeric form and structural features.

Check Digit Verification of cas no

The CAS Registry Mumber 1785-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1785-55:
(6*1)+(5*7)+(4*8)+(3*5)+(2*5)+(1*5)=103
103 % 10 = 3
So 1785-55-3 is a valid CAS Registry Number.

1785-55-3Downstream Products

1785-55-3Relevant academic research and scientific papers

Activation of unsaturated substrates by cobalt complexes. Crystal structure and reactivity of a complex of octacarbonyl dicobalt with N-methylbis(α,α-dimethylpropargyl)amine

Battaglia, Luigi Pietro,Delledonne, Daniele,Nardelli, Mario,Predieri, Giovanni,Chiusoli, Gian Paolo,et al.

, p. 209 - 222 (2007/10/02)

A new complex of octacarbonyl dicobalt with N-methyl(α,α-dimethylpropargyl)amine was prepared and characterized by spectroscopic and X-ray diffraction methods.Each triple bond is coordinated to a hexacarbonyldicobalt fragment and each metal shows a pseudo-octahedral geometry.The structure of the free ligand having NH in place of N-methyl has also been determined for comparison.Thermal decomposition of the complex in toluene or in benzonitrile afforded a series of products, mainly resulting from the rearrangement of the original complex to a metallacyclic structure, able to incorporate either the acetylenic triple bond or carbon monoxide in the case of toluene and either the acetylenic or the nitrile triple bond in the case of benzonitrile.C-N bond cleavage of the starting amine was observed as a side reaction.Catalytic reactions leading to benzonitrile incorporation were also observed.A cross experiment with a 1/1 mixture of diynes, either with or without geminal methyl groups α to triple bonds showed that for conformation reasons the metallacycle moiety mainly comes from the substrate containing geminal groups, whilst for steric reasons the other substrate is preferentially incorporated into the metallacycle.

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