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2,7-Dibromo-9,10-dihydroacridine-9-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10352-14-4 Structure
  • Basic information

    1. Product Name: 2,7-Dibromo-9,10-dihydroacridine-9-one
    2. Synonyms: 2,7-Dibromo-9,10-dihydroacridine-9-one;2,7-Dibromoacridin-9(10H)-one;2,7-Dibromoacridone
    3. CAS NO:10352-14-4
    4. Molecular Formula: C13H7Br2NO
    5. Molecular Weight: 353.01
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10352-14-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,7-Dibromo-9,10-dihydroacridine-9-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,7-Dibromo-9,10-dihydroacridine-9-one(10352-14-4)
    11. EPA Substance Registry System: 2,7-Dibromo-9,10-dihydroacridine-9-one(10352-14-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 10352-14-4(Hazardous Substances Data)

10352-14-4 Usage

Uses

2,7-Dibromoacridone is used in the systhesis of series of acridinium photocatalysts.

Check Digit Verification of cas no

The CAS Registry Mumber 10352-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,5 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10352-14:
(7*1)+(6*0)+(5*3)+(4*5)+(3*2)+(2*1)+(1*4)=54
54 % 10 = 4
So 10352-14-4 is a valid CAS Registry Number.

10352-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-dibromo-10H-acridin-9-one

1.2 Other means of identification

Product number -
Other names 2,7-dibromoacridone

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:10352-14-4 SDS

10352-14-4Relevant articles and documents

Reactions of π-deficient aromatic heterocycles with ammonium polyhalides. I. Halogenation of acridone and acridine derivatives using benzyltriethylammonium (BTEA) polyhalides

Vlassa,Silberg,Custelceanu,Culea

, p. 3493 - 3501 (1995)

The reactions of acridine and acridone with benzyltriethylammonium polyhalides in various solvents, under mild conditions, gave mono- and dihalogenated acridine and acridone derivatives and acridine complexes in good yields.

Compound as well as light-emitting device and display device thereof

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Paragraph 0153; 0154; 0155; 0156, (2018/01/03)

The invention relates to the technical field of organic light-emitting materials and in particular relates to a compound as well as a light-emitting device and a display device thereof. A structural formula of the compound is shown as a general formula I. The invention provides a TADF (Thermally Activated Delayed Fluorescence) material based on a tetraphenylethylene structure and the TADF material has TADF and AIE (Aggregation-Induced Emission) effects; a traditional fluorescent molecule transition forbidden triple-state exciton can be used for emitting light, and exciton quenching under high current density and doping concentration can also be avoided, so that the efficiency of the device can be remarkably improved. (The formula I is shown in the description.).

Bridged Organosilane and Production Method Thereof

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Page/Page column 28-29, (2009/04/24)

Provided is a bridged organosilane, which has a large complex organic group, and which is useful in the synthesis of a mesoporous silica and a light-emitting material, and a production method of the bridged organosilane. The bridged organosilane is expressed by the following general formula (1): [in the formula (1), q represents an integer in a range from 2 to 4, X1— represents a substituent selected from the group consisting of substituents expressed by the following general formulae (2) to (5): (in the formulae (2) to (5), R1 represents alkyl group having 1 to 5 carbon atoms, R2 represents an allyl group, and n represents an integer in a range from 0 to 3, and m represents an integer in a range from 0 to 6), and A1 represents an organic group expressed by, for example, the following general formula (6): (in the formula (6), Y1 represents a substituent expressed by, for example, O═C)].

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