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1H-Inden-1-one,2,3-dihydro-4-hydroxy-5-nitro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

375825-59-5

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375825-59-5 Usage

General Description

1H-Inden-1-one, 2,3-dihydro-4-hydroxy-5-nitro-(9CI) is a chemical compound with the molecular formula C9H7NO4. It is a nitro-substituted indenone derivative with a hydroxy group attached to the fourth carbon and a nitro group attached to the fifth carbon of the indenone ring. 1H-Inden-1-one,2,3-dihydro-4-hydroxy-5-nitro-(9CI) is a yellow crystalline solid that is insoluble in water but soluble in organic solvents. It is used in the synthesis of pharmaceuticals, dyes, and other organic compounds. The presence of the nitro and hydroxy functional groups in 1H-Inden-1-one,2,3-dihydro-4-hydroxy-5-nitro-(9CI) makes it suitable for various chemical reactions and applications in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 375825-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,5,8,2 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 375825-59:
(8*3)+(7*7)+(6*5)+(5*8)+(4*2)+(3*5)+(2*5)+(1*9)=185
185 % 10 = 5
So 375825-59-5 is a valid CAS Registry Number.

375825-59-5SDS

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-hydroxy-5-nitro-2,3-dihydroinden-1-one

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-5-Nitro-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:375825-59-5 SDS

375825-59-5Downstream Products

375825-59-5Relevant academic research and scientific papers

Iodine(III)-Catalyzed Electrophilic Nitration of Phenols via Non-Br?nsted Acidic NO2+ Generation

Juárez-Ornelas, Kevin A.,Jiménez-Halla, J. Oscar C.,Kato, Terumasa,Solorio-Alvarado, César R.,Maruoka, Keiji

supporting information, p. 1315 - 1319 (2019/03/07)

The first catalytic procedure for the electrophilic nitration of phenols was developed using iodosylbenzene as an organocatalyst based on iodine(III) and aluminum nitrate as a nitro group source. This atom-economic protocol occurs under mild, non-Br?nsted acidic and open-flask reaction conditions with a broad functional-group tolerance including several heterocycles. Density functional theory (DFT) calculations at the (SMD:MeCN)Mo8-HX/(LANLo8+f,6-311+G) level indicated that the reaction proceeds through a cationic pathway that efficiently generates the NO2+ ion, which is the nitrating species under neutral conditions.

CARBAZOLE COMPOUNDS AND METHODS OF USING SAME

-

Paragraph 00125, (2015/02/25)

The present invention provides carbazole compounds of the formula (I), which can be used for treating microbial, protozoan, viral infections and cancer. ?

FUSED INDOLE COMPOUNDS AND METHODS OF USING SAME

-

Paragraph 00122; 00123, (2015/04/22)

The invention relates to fused indole compounds of formula (I) that can be used for treating microbial infections, in particular, fungal infections, and selectively kill cancer cells.

CARBAZOLE COMPOUNDS AND METHODS OF USING SAME

-

Paragraph 00118; 00119, (2015/04/22)

The invention relates to carbazole compounds of formula (I) that can be used for treating microbial infections, in particular, fungal infections, and selectively kill cancer cells.

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