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9H-Fluoren-9-one, 6-bromo-2-methyl- is a chemical compound with the molecular formula C13H9BrO and a molecular weight of 257.11 g/mol. It is a derivative of fluorenone, a tricyclic aromatic ketone, with a bromine atom at the 6-position and a methyl group at the 2-position. 9H-Fluoren-9-one, 6-bromo-2-methyl- is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is characterized by its white crystalline appearance and is soluble in common organic solvents. Due to its reactivity, it is essential to handle 9H-Fluoren-9-one, 6-bromo-2-methyl- with care, following proper safety protocols and guidelines.

137154-53-1

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137154-53-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137154-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,1,5 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 137154-53:
(8*1)+(7*3)+(6*7)+(5*1)+(4*5)+(3*4)+(2*5)+(1*3)=121
121 % 10 = 1
So 137154-53-1 is a valid CAS Registry Number.

137154-53-1SDS

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 6-bromo-2-methylfluoren-9-one

1.2 Other means of identification

Product number -
Other names 9H-Fluoren-9-one,6-bromo-2-methyl

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:137154-53-1 SDS

137154-53-1Upstream product

137154-53-1Relevant academic research and scientific papers

Intramolecular aromatic 1,5-hydrogen transfer in free radical reactions. II. Rearrangement of iodobenzophenones

Cummins, Jordan M.,Dolling, Ulf-H.,Douglas, Alan W.,Karady, Sandor,Leonard Jr., William R.,Marcune, Benjamin F.

, p. 6153 - 6156 (2007/10/03)

Products derived from the homolysis of the aromatic C-I bond of ortho- iodobenzophenones by photolysis or tributyltin radicals indicate 1,5-hydrogen migration. The reactions include iodine migration, hydrogen abstraction and arylation.

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