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4,7-dihydro-1-Methyl-4,7-Ethano-2H-isoindole, also known as tetrahydroalstophylline, is a chemical compound with a complex molecular structure consisting of an isoindole ring fused to a cyclopropane ring, with a methyl group attached at the 1-position. It is a derivative of the alkaloid alstophylline and has been studied for its potential pharmaceutical properties, particularly for its potential use as a neuroprotective and cognition-enhancing agent. Its unique structure allows it to interact with various receptors and enzymes in the brain, making it a subject of interest for potential therapeutic applications in the treatment of neurological and neuropsychiatric disorders. Its synthesis and pharmacological properties are ongoing topics of research in the field of medicinal chemistry.

357608-23-2

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357608-23-2 Usage

Uses

Used in Pharmaceutical Industry:
4,7-dihydro-1-Methyl-4,7-Ethano-2H-isoindole is used as a neuroprotective and cognition-enhancing agent for its potential therapeutic applications in the treatment of neurological and neuropsychiatric disorders. Its unique structure allows it to interact with various receptors and enzymes in the brain, making it a promising candidate for the development of new drugs to address these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 357608-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,6,0 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 357608-23:
(8*3)+(7*5)+(6*7)+(5*6)+(4*0)+(3*8)+(2*2)+(1*3)=162
162 % 10 = 2
So 357608-23-2 is a valid CAS Registry Number.

357608-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Methyl-4,7-dihydro-2H-4,7-ethanoisoindole

1.2 Other means of identification

Product number -
Other names 4,7-ethano-4,7-dihydro-3-methylisoindole

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:357608-23-2 SDS

357608-23-2Downstream Products

357608-23-2Relevant academic research and scientific papers

Synthesis and properties of novel extended BODIPYs with rigid skeletons

Kawamata, Yuki,Ito, Satoshi,Furuya, Masaru,Takahashi, Kai,Namai, Katsuya,Hashimoto, Saori,Roppongi, Makoto,Oba, Toru

, p. 707 - 712 (2019)

Novel extended BODIPYs fused with bicyclo rings were synthesized from bicyclopyrroles by combining Knoevenagel condensation, Suzuki coupling, and O-chelation. The absorption maxima of the BODIPYs ranged from the visible to near-infrared region and the compounds showed good solubility in organic solvents. The solubility of the bicycloBODIPY with 2-naphthyl groups at the α-position of the pyrrole units was particularly high. Heating converted distyrylBODIPY with bicyclo[2.2.2]octene to benzoBODIPY with absorption (748.5 nm) and fluorescence (775.0 nm) in the near-infrared region.

Boron-diindomethene (BDI) dyes and their tetrahydrobicyclo precursors - En route to a new class of highly emissive fluorophores for the red spectral range

Shen, Zhen,Roehr, Holger,Rurack, Knut,Uno, Hidemitsu,Spieles, Monika,Schulz, Burkhard,Reck, Guenter,Ono, Noboru

, p. 4853 - 4871 (2004)

The X-ray crystallographic, optical spectroscopic, and electrochemical properties of a newly synthesized class of boron-diindomethene (BDI) dyes and their tetrahydrobicyclo precursors (bc-BDP) are presented. The BDI chromophore was designed to show intens

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