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6-BROMO-2,3-DIHYDRO-1H-INDENE-1-CARBONITRILE is a chemical compound characterized by the molecular formula C11H8BrN. It is an indene derivative that incorporates a bromine atom and a cyano group within its structure. 6-BROMO-2,3-DIHYDRO-1H-INDENE-1-CARBONITRILE is recognized for its distinctive chemical properties and reactivity, which render it a valuable asset in the realms of organic synthesis and pharmaceutical research.

783335-58-0

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783335-58-0 Usage

Uses

Used in Organic Synthesis:
6-BROMO-2,3-DIHYDRO-1H-INDENE-1-CARBONITRILE serves as a versatile building block in organic synthesis, facilitating the creation of more complex organic molecules. Its unique structure and reactivity make it a promising candidate for the development of novel chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 6-BROMO-2,3-DIHYDRO-1H-INDENE-1-CARBONITRILE is utilized as a precursor in the formulation of new drugs. Its potential biological activity and capacity to be modified into various drug-like molecules contribute to its significance in drug discovery and development processes.
Used in Medical Field:
6-BROMO-2,3-DIHYDRO-1H-INDENE-1-CARBONITRILE may exhibit biological activity that could be harnessed in the medical field. Its specific interactions with biological systems could lead to the discovery of new therapeutic agents or diagnostic tools.
Used in Agricultural Field:
Similarly, in agriculture, the compound's biological activity might be relevant for the development of new pesticides, herbicides, or other agrochemicals, thereby contributing to more effective and targeted crop protection strategies.
Overall, 6-BROMO-2,3-DIHYDRO-1H-INDENE-1-CARBONITRILE is a multifaceted chemical compound with a broad spectrum of potential applications across different industries, underscoring its value in scientific and commercial domains.

Check Digit Verification of cas no

The CAS Registry Mumber 783335-58-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,3,3,3 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 783335-58:
(8*7)+(7*8)+(6*3)+(5*3)+(4*3)+(3*5)+(2*5)+(1*8)=190
190 % 10 = 0
So 783335-58-0 is a valid CAS Registry Number.

783335-58-0SDS

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 6-bromo-2,3-dihydro-1H-indene-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 6-bromoindan-1-carbonitrile

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:783335-58-0 SDS

783335-58-0Relevant articles and documents

COMPOUNDS AND USES THEREOF

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Page/Page column 227-228, (2021/08/06)

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

Aryl alkylamine compound, preparation method thereof and application of aryl alkylamine compound in medicines

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Paragraph 0480-0485, (2021/07/17)

The invention relates to an aryl alkylamine compound, a preparation method thereof and application of the aryl alkylamine compound in medicines. Particularly, the compound disclosed by the invention is suitable for being used as a calcium-sensitive recept

COMPOUNDS AND USES THEREOF

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Page/Page column 71; 93-94, (2021/08/06)

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

Synthesis of chloro and bromo substituted 5-(indan-1′-yl)tetrazoles and 5-(indan-1′-yl)methyltetrazoles as possible analgesic agents

Bachar, Sitesh Chandra,Lahiri

, p. 435 - 438 (2007/10/03)

Chloro and bromo substututed indanyl tetrazoles (compounds 5a, b) and indanyl methyltetrazoles (compounds 5c, 5d) have been synthesized from their respective acids through amide and nitrile routes, and characterized. The title compounds (5a, 5b, 5c and 5d) were subjected for their analgesic activity in the acetic acid induced writhing test on albino mice. The significant (p chlorine and tetrazole > methyltetrazole.

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