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4-Bromo-2,3-dihydro-1H-indene, a brominated derivative of 2,3-dihydro-1H-indene, is a bicyclic organic compound with the molecular formula C9H9Br. It is a flammable liquid characterized by a strong, unpleasant odor and potential health hazards and environmental impacts. Due to its chemical properties, it is commonly used as a building block in organic synthesis for the production of pharmaceuticals, agrochemicals, and other organic compounds.

6134-53-8

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6134-53-8 Usage

Uses

Used in Pharmaceutical Industry:
4-Bromo-2,3-dihydro-1H-indene is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 4-Bromo-2,3-dihydro-1H-indene serves as a precursor for the production of various agrochemicals, including pesticides and herbicides. Its versatility in organic synthesis enables the creation of effective and targeted agrochemicals for agricultural use.
Used in Organic Synthesis:
4-Bromo-2,3-dihydro-1H-indene is utilized as a building block in organic synthesis for the development of a wide range of organic compounds. Its reactivity and structural properties make it a valuable component in the synthesis of complex organic molecules for various applications.
It is crucial to handle 4-Bromo-2,3-dihydro-1H-indene with caution, adhering to safety guidelines and consulting relevant safety data sheets and regulations to minimize potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 6134-53-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,3 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6134-53:
(6*6)+(5*1)+(4*3)+(3*4)+(2*5)+(1*3)=78
78 % 10 = 8
So 6134-53-8 is a valid CAS Registry Number.

6134-53-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromo-2,3-dihydro-1H-indene

1.2 Other means of identification

Product number -
Other names 4-Brom-indan

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:6134-53-8 SDS

6134-53-8Relevant articles and documents

Aromatic amine derivative organic electroluminescent material and device thereof

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Paragraph 0311-0315, (2021/11/26)

The invention discloses an aromatic amine derivative organic electroluminescent material and a device thereof. The compound is a pyrene compound substituted with an aromatic amine, wherein the compound has a substituted or unsubstituted (hetero) aryl group and a pyrene compound substituted or unsubstituted aromatic amine structure of a (hetero) aryl group, which may be used as a light emitting material in an organic electroluminescent device. These novel compounds can provide better device performance, such as higher external quantum efficiency and narrower half-peak widths, and the like.

INFLUENZA VIRUS REPLICATION INHIBITOR AND USES THEREOF

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Paragraph 00190; 00317-00318, (2020/05/21)

The invention belongs to the field of medicine, and particularly relates to a novel compound as a replication inhibitor of influenza virus and a preparation method thereof, a pharmaceutical composition comprising the compound and use of the compound and pharmaceutical composition thereof in treating influenza. The present invention provides a compound having Formula (I) or a stereoisomer, a tautomer, an N-oxide, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof, The compound of the present invention can inhibit influenza virus well, and/or has lower cytotoxicity, better in vivo pharmacokinetic properties and in vivo pharmacodynamic properties.

SHMT INHIBITORS AND USES THEREOF

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Paragraph 00232, (2018/06/30)

The present invention provides compounds, compositions thereof, and methods of using the same.

NOVEL NEUROKININ 1 RECEPTOR ANTAGONIST COMPOUNDS II

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Page/Page column 110, (2015/03/13)

The invention relates novel NK1 receptor antagonists represented in formula A, wherein R1 and R2 independently are selected from the group consisting of (C1-4)alkyl, (C1-4)haloalkyl, (C1-4)alkoxy, CD

FUSED HETEROCYCLIC COMPOUNDS AND THROMBOPOIETIN RECEPTOR ACTIVATORS

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Page/Page column 32, (2012/08/28)

Fused heterocyclic compounds useful for prevention, treatment or improvement of diseases against which activation of the thrombopoietin receptor is effective are provided. A compound represented by the formula (I) (wherein R1 is an aryl group fused to a saturated ring or the like, A, B, L1, R2, L2, L3, Y, L4, R3 and X are defined in the description), a tautomer, prodrug or a pharmaceutically acceptable salt of the compound or a solvate thereof.

SUBSTITUTED PARA-BIPHENYLOXYMETHYL DIHYDRO OXAZOLOPYRIMIDINONES, PREPARATION AND USE THEREOF

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Page/Page column 44, (2011/04/19)

The present invention relates to a series of substituted para-biphenyloxymethyl dihydro oxazolopyrimidinones of formula (I) as defined herein. This invention also relates to methods of making these compounds including novel intermediates. The compounds of

Anti-cancer agents and uses thereof

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Page/Page column 27, (2008/12/08)

The present invention is in the area of novel compounds and salts thereof, their syntheses, and their use as anti-cancer agents. The compounds include compounds of Formula I: and solvates, hydrates and pharmaceutically-acceptable salts thereof, wherein A1 is N or CR1; A3 is N or CR3; A5 is N or CR5; R1, R3-R6 and L are defined in the specification; n is 0 or 1; and X is an optionally-substituted aryl group having 6-10 carbons in the ring portion, an optionally-substituted 6-membered heteroaryl group having 1-3 nitrogen atoms in the ring portion, an optionally-substituted 5-membered heteroaryl group having 0-4 nitrogen atoms in the ring portion and optionally having 1 sulfur atom or 1 oxygen atom in the ring portion, or an optionally-substituted heteroaryl group in which a 6-membered ring is fused either to a 5-membered ring or to a 6-membered ring, wherein in each case 1, 2, 3 or 4 ring atoms are heteroatoms independently selected from nitrogen, oxygen and sulfur. They are effective against a broad range of cancers, especially leukemia, prostate, non-small cell lung and colon. They are additionally useful in the treatment of proliferative retinopathies such as diabetic neuropathy and macular degeneration.

Anti-cancer agents and uses thereof

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Page/Page column 27, (2008/06/13)

The present invention is in the area of novel compounds and salts thereof, their syntheses, and their use as anti-cancer agents. The compounds include compounds of Formula I: and solvates, hydrates and pharmaceutically-acceptable salts thereof, wherein A1 is N or CR1; A3 is N or CR3; A5 is N or CR5; R1, R3—R6 and L are defined in the specification; n is 0 or 1; and X is an optionally-substituted aryl group having 6-10 carbons in the ring portion, an optionally-substituted 6-membered heteroaryl group having 1-3 nitrogen atoms in the ring portion, an optionally-substituted 5-membered heteroaryl group having 0-4 nitrogen atoms in the ring portion and optionally having 1 sulfur atom or 1 oxygen atom in the ring portion, or an optionally-substituted heteroaryl group in which a 6-membered ring is fused either to a 5-membered ring or to a 6-membered ring, wherein in each case 1, 2, 3 or 4 ring atoms are heteroatoms independently selected from nitrogen, oxygen and sulfur. They are effective against a broad range of cancers, especially leukemia, non-small cell lung and colon.

A simple and improved procedure for selective ring bromination of alkyl-substituted aromatic hydrocarbons on the surface of alumina

Ranu,Sarkar,Chakraborty

, p. 1095 - 1099 (2007/10/02)

Highly selective ring bromination of alkyl-substituted aromatic hydrocarbons has been achieved using molecular bromine adsorbed on the surface of alumina without any solvent.

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