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5-Iodo-2,3-dihydro-1H-isoindole is a chemical compound characterized by the molecular formula C8H7IN. It is an isoindole derivative featuring an iodo substituent at the 5-position, which endows it with unique chemical properties and reactivity. This versatile compound is recognized for its potential in various fields of chemical research, including medicinal chemistry and material science.

905274-25-1

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905274-25-1 Usage

Uses

Used in Organic Synthesis:
5-Iodo-2,3-dihydro-1H-isoindole serves as a valuable building block in organic synthesis, contributing to the creation of a wide array of biologically active compounds. Its presence in these syntheses is instrumental for the development of new pharmaceutical agents and other organic molecules with specific applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-Iodo-2,3-dihydro-1H-isoindole is utilized as a key component in the synthesis of drugs. Its unique structure allows for the exploration of new chemical entities that could address unmet medical needs, offering a promising avenue for the discovery of novel therapeutics.
Used as a Reagent in Chemical Reactions:
5-Iodo-2,3-dihydro-1H-isoindole also functions as a reagent in various chemical reactions, facilitating the formation of complex organic molecules. Its reactivity, particularly due to the iodo substituent, makes it a useful tool in the synthesis of target compounds with specific properties.
Used in Material Science:
5-Iodo-2,3-dihydro-1H-isoindole's potential extends to material science, where it may be employed in the development of new materials with unique properties. Its structural features could contribute to the creation of advanced materials for various applications, such as in electronics or as components of new technologies.
Used as a Starting Material for Complex Organic Molecule Synthesis:
5-Iodo-2,3-dihydro-1H-isoindole is recognized as a starting material for the synthesis of complex organic molecules. Its role in these syntheses is crucial for constructing intricate molecular architectures that can exhibit specialized functions or properties in different chemical and biological contexts.

Check Digit Verification of cas no

The CAS Registry Mumber 905274-25-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,2,7 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 905274-25:
(8*9)+(7*0)+(6*5)+(5*2)+(4*7)+(3*4)+(2*2)+(1*5)=161
161 % 10 = 1
So 905274-25-1 is a valid CAS Registry Number.

905274-25-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-iodo-2,3-dihydro-1H-isoindole

1.2 Other means of identification

Product number -
Other names 2,3-DIHYDRO-5-IODO-1H-ISOINDOLE

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:905274-25-1 SDS

905274-25-1Upstream product

905274-25-1Downstream Products

905274-25-1Relevant academic research and scientific papers

Inhibitors of dipeptidyl peptidase 8 and dipeptidyl peptidase 9. Part 2: Isoindoline containing inhibitors

Van Goethem, Sebastiaan,Van der Veken, Pieter,Dubois, Veronique,Soroka, Anna,Lambeir, Anne-Marie,Chen, Xin,Haemers, Achiel,Scharpe, Simon,De Meester, Ingrid,Augustyns, Koen

, p. 4159 - 4162 (2008)

To obtain selective and potent inhibitors of dipeptidyl peptidases 8 and 9, we synthesized a series of substituted isoindolines as modified analogs of allo-Ile-isoindoline, the reference DPP8/9 inhibitor. The influence of phenyl substituents and different P2 residues on the inhibitors' affinity toward other DPPs and more specifically, their potential to discriminate between DPP8 and DPP9 will be discussed. Within this series compound 8j was shown to be a potent and selective inhibitor of DPP8/9 with low activity toward DPP II.

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