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6292-55-3

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6292-55-3 Usage

General Description

3-acetylaminofluorene is a chemical compound that is often used in research as a potent carcinogen. It is a derivative of aminofluorene, a known mutagen, and has been shown to induce tumors in various animal models. 3-acetylaminofluorene is commonly employed in studies to investigate the mechanisms of chemical carcinogenesis and to develop new treatments for cancer. It is also utilized to assess the effectiveness of chemopreventive agents in inhibiting the formation of tumors. Due to its carcinogenic properties, 3-acetylaminofluorene is considered a hazardous substance and is strictly regulated in research and industrial settings.

Check Digit Verification of cas no

The CAS Registry Mumber 6292-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6292-55:
(6*6)+(5*2)+(4*9)+(3*2)+(2*5)+(1*5)=103
103 % 10 = 3
So 6292-55-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H13NO/c1-10(17)16-13-7-6-12-8-11-4-2-3-5-14(11)15(12)9-13/h2-7,9H,8H2,1H3,(H,16,17)

6292-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(9H-fluoren-3-yl)acetamide

1.2 Other means of identification

Product number -
Other names 2-acetylaminofluorene

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:6292-55-3 SDS

6292-55-3Downstream Products

6292-55-3Relevant articles and documents

A novel construction of acetamides from rhodium-catalyzed aminocarbonylation of DMC with nitro compounds

Bao, Zhi-Peng,Miao, Ren-Guan,Qi, Xinxin,Wu, Xiao-Feng

supporting information, p. 1955 - 1958 (2021/03/02)

Dimethyl carbonate (DMC), an environment-friendly compound prepared from CO2, shows diverse reactivities. In this communication, an efficient procedure using DMC as both a C1 building block and solvent in the aminocarbonylation reaction with nitro compounds has been developed. W(CO)6acts both a CO source and a reductant here.

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