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6-Bromo-4-isochromanone is a heterocyclic compound characterized by a six-membered ring structure that includes oxygen and bromine atoms. It is recognized for its potential as a building block in the synthesis of pharmaceutical and organic compounds, with notable biological activities such as inhibiting cancer cell growth, antifungal properties, and neuroprotective capabilities.

676134-68-2

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676134-68-2 Usage

Uses

Used in Pharmaceutical Synthesis:
6-Bromo-4-isochromanone is used as a key building block for the synthesis of various pharmaceutical compounds due to its unique structural features and reactivity, contributing to the development of new drugs with diverse therapeutic potentials.
Used in Organic Chemistry:
In the field of organic chemistry, 6-Bromo-4-isochromanone serves as a valuable starting material for the synthesis of novel compounds, enabling researchers to explore its chemical properties and applications in creating new organic molecules with potential uses.
Used in Cancer Research:
6-Bromo-4-isochromanone is utilized as a research compound in cancer studies for its ability to inhibit the growth of cancer cells. It is investigated for its potential as an anticancer agent, providing insights into its mechanisms of action and possible integration into cancer treatment strategies.
Used in Antifungal Applications:
6-Bromo-4-isochromanone is also used in antifungal research, where its properties are studied to combat fungal infections. The exploration of its antifungal capabilities can lead to the development of new antifungal agents for medical and agricultural use.
Used in Neuroprotective Research:
6-Bromo-4-isochromanone is employed in neuroprotective studies, where its potential to protect neurons and mitigate neurodegenerative effects is investigated. This research could contribute to the advancement of treatments for neurological disorders.
Overall, 6-Bromo-4-isochromanone is a versatile chemical compound with a broad spectrum of applications across various industries, particularly in medicine and organic chemistry, due to its unique structure and biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 676134-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,1,3 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 676134-68:
(8*6)+(7*7)+(6*6)+(5*1)+(4*3)+(3*4)+(2*6)+(1*8)=182
182 % 10 = 2
So 676134-68-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H7BrO2/c10-7-2-1-6-4-12-5-9(11)8(6)3-7/h1-3H,4-5H2

676134-68-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-1H-isochromen-4-one

1.2 Other means of identification

Product number -
Other names 6-Bromo-4-Isochromanone

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:676134-68-2 SDS

676134-68-2Downstream Products

676134-68-2Relevant academic research and scientific papers

COMPOUNDS AND USES THEREOF

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, (2021/08/06)

The present disclosure features compounds useful for the treatment of BAF complex-related disorders.

COMPOUNDS AND USES THEREOF

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, (2021/08/06)

The present disclosure features compounds useful for the treatment of BAF complex-related disorders.

METHODS OF TREATMENT OF AMYLOIDOSIS USING BI-CYCLIC ASPARTYL PROTEASE INHIBITORS

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Page/Page column 267, (2010/02/14)

The invention relates to novel compounds and methods of treating diseases, disorders, and conditions associated with amyloidosis. Amyloidosis refers to a collection of diseases, disorders, and conditions associated with abnormal deposition of A-beta protein.

2-AMINO- AND 2-THIO-SUBSTITUTED 1,3-DIAMINOPROPANES

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Page/Page column 162-163, (2008/06/13)

Disclosed are compounds of the formula: where variables Q, Z, X, R15, R2, R3, and Rc are defined herein. Compounds disclosed herein are inhibitors of the beta-secretase enzyme and are therefore useful in the treatment of Alzheimer’s disease and other diseases characterized by deposition of A beta peptide in a mammal.

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