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22250-99-3

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22250-99-3 Usage

Chemical Class

Nitroaromatic compounds

Physical Form

Yellow crystalline solid

Usage

Organic synthesis, research chemical

Mutagenicity

Potent mutagen

Carcinogenicity

Potential human carcinogen

Toxicity

Toxic to aquatic organisms

Environmental Impact

May cause long-term adverse effects in the aquatic environment

Handling and Disposal

Proper handling and disposal is important to minimize its impact on the environment and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 22250-99-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,5 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22250-99:
(7*2)+(6*2)+(5*2)+(4*5)+(3*0)+(2*9)+(1*9)=83
83 % 10 = 3
So 22250-99-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H9NO2/c15-14(16)13-7-3-6-11-10-5-2-1-4-9(10)8-12(11)13/h1-7H,8H2

22250-99-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-nitro-9H-fluorene

1.2 Other means of identification

Product number -
Other names 9H-Fluorene,1-nitro

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:22250-99-3 SDS

22250-99-3Relevant 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 (2007/10/02)

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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