6630-65-5

Usage

Uses

Used in Agricultural Applications:
9-Chlorofluorene is used as a fungicide for the treatment of fungal diseases in tomato plants. Its application helps protect the plants from infections and enhances their overall health and yield.
Used in Environmental Studies:
9-Chlorofluorene is also used in environmental studies as an example of halogenated pollutants. Understanding its presence and impact in the urban atmosphere can contribute to the development of strategies for reducing air pollution and protecting public health.

InChI:InChI=1/C13H9Cl/c14-13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)13/h1-8,13H

Upstream product

• 105878-62-4 1-(9H-Fluoren-9-yl)-pyridinium; chloride 
• 7647-01-0 hydrogenchloride 
• 25017-68-9 9-acetoxy-9H-fluorene 
• 15719-64-9 methylammonium carbonate 
• 56-23-5 tetrachloromethane 
• 13629-22-6 fluoren-9-ylidene-hydrazine 
• 1689-64-1 9-Fluorenol 

Downstream Products

• 1530-12-7 9,9'-bifluorenyl 
• 1989-33-9 9H-fluorene-9-carboxylic acid 
• 101796-83-2 difluoren-9-yl disulfide 
• 4364-32-3 9-(4,4'-bis-dimethylamino-benzhydrylidene)-fluorene 
• 83463-89-2 bis-(4,4'-bis-dimethylamino-benzhydryl)-disulfide 
• 70383-91-4 fluoren-9-one-[N-(4-dimethylamino-phenyl)-oxime ] 
• 632-50-8 1,1,2,2-tetraphenylethane 
• 4425-68-7 9-(diphenylmethyl)fluorene 
• 2841-40-9 9-phenylethynylfluorene 
• 855600-13-4 1-fluoren-9-yl-2-oxo-cyclohexanecarboxylic acid ethyl ester 
• 486-25-9 9-fluorenone 
• 13629-22-6 fluoren-9-ylidene-hydrazine 
• 746-47-4 tetrabenzo[5.5]fulvalene 
• 24040-37-7 9-azido-9H-fluorene 

Relevant academic research and scientific papers

Deoxygenation of benzylic alcohols using chloroboranes

New boron-based methods for deoxygenating benzylic alcohols via the corresponding alkoxides are reported.

Catalytic olefination of carbonyl compounds. Effect of the structure of the carbonyl compound on the reaction

The mechanism of the novel reaction of catalytic olefination of carbonyl compounds was studied. The reaction involves the transformation of hydrazones of aromatic aldehydes and ketones into the corresponding dichloroalkenes and symmetrical azines by the treatment with carbon tetrachloride in the presence of CuCl as a catalyst. The stability of intermediate diazoalkanes is the main factor determining the direction of the reaction. In the case of sufficiently stable diazoalkanes, other products can be formed under the reaction conditions along with the products of catalytic olefination.