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4-Chloro-2,3-dihydro-7-methyl-1H-inden-1-one is a chemical compound characterized by the molecular formula C10H9ClO. It is a white solid that exhibits solubility in organic solvents but is insoluble in water. 4-Chloro-2,3-dihydro-7-methyl-1H-inden-1-one is recognized for its role in the synthesis of other chemical compounds and pharmaceuticals, and it serves as a valuable building block in the production of various organic molecules. Its unique structure and properties also suggest potential applications in medicine and agrochemicals, although it requires careful handling due to its potential hazards.

5333-90-4

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5333-90-4 Usage

Uses

Used in Chemical Synthesis:
4-Chloro-2,3-dihydro-7-methyl-1H-inden-1-one is used as a key intermediate in the synthesis of other chemical compounds, facilitating the creation of a diverse range of products.
Used in Pharmaceutical Production:
4-Chloro-2,3-dihydro-7-methyl-1H-inden-1-one is utilized as a building block in the development of pharmaceuticals, contributing to the formulation of new drugs and medicines.
Used in Research and Development:
4-Chloro-2,3-dihydro-7-methyl-1H-inden-1-one is employed in research settings as a fundamental component in the production of various organic molecules, aiding in scientific discovery and innovation.
Used in Medicine:
Due to its unique structure and properties, 4-Chloro-2,3-dihydro-7-methyl-1H-inden-1-one may have potential applications in the medical field, although further research is necessary to explore its specific uses and efficacy.
Used in Agrochemicals:
4-Chloro-2,3-dihydro-7-methyl-1H-inden-1-one may also find use in the agrochemical industry, potentially contributing to the development of new pesticides or other agricultural chemicals, again highlighting the need for further investigation into its applicability and safety.

Check Digit Verification of cas no

The CAS Registry Mumber 5333-90-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5333-90:
(6*5)+(5*3)+(4*3)+(3*3)+(2*9)+(1*0)=84
84 % 10 = 4
So 5333-90-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClO/c1-6-2-4-8(11)7-3-5-9(12)10(6)7/h2,4H,3,5H2,1H3

5333-90-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-7-methyl-2,3-dihydroinden-1-one

1.2 Other means of identification

Product number -
Other names 4-Chloro-7-methyl-1-indanone

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:5333-90-4 SDS

5333-90-4Relevant academic research and scientific papers

Rh-Catalyzed Annulation of Benzoic Acids, Formaldehyde, and Malonates via ortho-Hydroarylation to Indanones

Yu, Shuling,Lv, Ningning,Hong, Chao,Liu, Zhanxiang,Zhang, Yuhong

supporting information, p. 8354 - 8358 (2020/11/18)

A three-component reaction from readily available low-cost materials of benzoic acids, formaldehyde, and malonates for the preparation of indanones by rhodium catalysis is reported. The annulation is initiated by an ortho-hydroarylation of benzoic acids, and a Lewis acid is not required. The solvent has a significant influence to the reaction, and 2-substituted or nonsubstituted indanones are obtained by the change of solvent.

SUBSTITUTED BENZOHYDRAZIDE ANALOGS AS HISTONE DEMETHYLASE INHIBITORS

-

, (2017/01/23)

Benzohydrazide analogs, derivatives thereof, and related compounds, which are useful as inhibitors of lysine-specific histone demethyfase, including LSD1 and LSD2; synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of using the compounds and compositions to treat disorders associated with dysfunction of the LSD1 and/or LSD2.

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