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2,3-dihydro-1H-benzo[f]isoindole, also known as tetrahydrobenzisoindole, is a bicyclic chemical compound with a benzo[f]isoindole core. It is an isoindoline that is frequently found in pharmaceutical and agrochemical products. 2,3-dihydro-1H-benzo[f]isoindole has been recognized for its potential medicinal properties, such as its analgesic and antipsychotic effects, and is utilized as a building block in the synthesis of various biologically active compounds. Furthermore, its insecticidal properties have positioned it as a candidate for use in insecticides and agricultural products.

6247-15-0

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6247-15-0 Usage

Uses

Used in Pharmaceutical Industry:
2,3-dihydro-1H-benzo[f]isoindole is used as a medicinal compound for its analgesic and antipsychotic properties, providing relief from pain and managing symptoms of psychological disorders.
Used in Agrochemical Industry:
2,3-dihydro-1H-benzo[f]isoindole is used as an insecticidal agent in agricultural products, helping to control and manage insect populations that can be detrimental to crops.
Used in Chemical Synthesis:
2,3-dihydro-1H-benzo[f]isoindole serves as a building block in the synthesis of biologically active compounds, contributing to the development of new pharmaceuticals and other chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 6247-15-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,4 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6247-15:
(6*6)+(5*2)+(4*4)+(3*7)+(2*1)+(1*5)=90
90 % 10 = 0
So 6247-15-0 is a valid CAS Registry Number.

6247-15-0Downstream Products

6247-15-0Relevant academic research and scientific papers

Chiral Supramolecular U-Shaped Catalysts Induce the Multiselective Diels-Alder Reaction of Propargyl Aldehyde

Hatano, Manabu,Sakamoto, Tatsuhiro,Mizuno, Tomokazu,Goto, Yuta,Ishihara, Kazuaki

, p. 16253 - 16263 (2018/11/27)

The Diels-Alder reaction, which is a traditional [4 + 2] cycloaddition with two carbon-carbon bond formations, is one of the most powerful tools to synthesize versatile and unique six-membered rings. We show that chiral supramolecular U-shaped boron Lewis acid catalysts promote the unprecedented multiselective Diels-Alder reaction of propargyl aldehyde with cyclic dienes. Independent from the substrate control, enantio-, endo/exo-, π-facial-, regio-, site-, and substrate-selectivities could be controlled by the present U-shaped catalysts. The obtained reaction products could access the concise synthesis of chiral diene ligands and a key intermediate of (+)-sarkomycin. The results presented here might partially contribute to the development of artificial enzyme-like supramolecular catalysts for multiselective reactions, which will be able to target organic compounds that have thus far eluded synthesis.

5-HT7 receptor antagonists

-

, (2008/06/13)

The present invention relates to compounds having pharmacological activity toward the 5-HT7receptor. Pharmaceutical compositions and methods for their use in the treatment of CNS disorders are described.

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