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124391-61-3

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124391-61-3 Usage

General Description

2-Aminofluorene is a chemical compound that consists of a fluorene molecule with an amino group attached to one of its carbon atoms. It is a white to pale yellow crystalline solid, and it is used in the production of dyes, pharmaceuticals, and as a research tool in the study of DNA damage and repair. 2-Aminofluorene is classified as a carcinogen and mutagen, as it can cause DNA damage and mutations, leading to an increased risk of cancer. It is considered a hazardous substance and should be handled with care, with proper protective equipment and in a well-ventilated area to minimize exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 124391-61-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,9 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124391-61:
(8*1)+(7*2)+(6*4)+(5*3)+(4*9)+(3*1)+(2*6)+(1*1)=113
113 % 10 = 3
So 124391-61-3 is a valid CAS Registry Number.

124391-61-3SDS

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 2-Aminofluorene

1.2 Other means of identification

Product number -
Other names 2-Hydroxymethyl-3-nitrobiphenyl

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:124391-61-3 SDS

124391-61-3Downstream Products

124391-61-3Relevant articles and documents

Regiospecific Syntheses of All Isomeric Nitrofluorenones and Nitrofluorenes by Transition Metal Catalyzed Cross-Coupling Reactions

Iihama, T.,Fu, J.-m.,Bourguignon, M.,Snieckus, V.

, p. 184 - 188 (1989)

Regiospecific efficient syntheses of 1-, 2-, 3-, and 4-nitrofluorenones 8 and the corresponding nitrofluorenes 10 by palladium(0)-catalyzed cross-coupling reactions of aryl boronic acids 1 with bromonitrotoluenes 2 and bromonitrobenzene 3 are described.

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