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ETHYL 3-FLUORO-4-NITROBENZOATE is a chemical compound with the molecular formula C9H6FNO4, belonging to the family of esters. It is a derivative of benzoic acid, characterized by the presence of a fluorine atom at the 3-position and a nitro group at the 4-position of the benzoate moiety. This unique structural feature makes it an important intermediate in the synthesis of bioactive molecules and it exhibits potential pharmacological activities.

914347-91-4

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914347-91-4 Usage

Uses

Used in Organic Synthesis:
ETHYL 3-FLUORO-4-NITROBENZOATE is used as a building block in the synthesis of various pharmaceutical compounds due to its unique structural features.
Used in Medicinal Chemistry:
It serves as an important intermediate in the preparation of bioactive molecules, contributing to the development of new drugs with potential pharmacological activities.
Used in the Production of Fine Chemicals:
ETHYL 3-FLUORO-4-NITROBENZOATE is utilized in the production of fine chemicals and specialty products, showcasing its versatility in different chemical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 914347-91-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,3,4 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 914347-91:
(8*9)+(7*1)+(6*4)+(5*3)+(4*4)+(3*7)+(2*9)+(1*1)=174
174 % 10 = 4
So 914347-91-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H8FNO4/c1-2-15-9(12)6-3-4-8(11(13)14)7(10)5-6/h3-5H,2H2,1H3

914347-91-4SDS

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 ETHYL 3-FLUORO-4-NITROBENZOATE

1.2 Other means of identification

Product number -
Other names 3-Fluoro-4-nitrobenzoic acid ethyl ester

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:914347-91-4 SDS

914347-91-4Relevant academic research and scientific papers

Vitamin B1-catalyzed aerobic oxidative esterification of aromatic aldehydes with alcohols

Chu, Xue-Qiang,Ge, Danhua,Luo, Xin-Long,Xu, Pei,Yu, Zi-Lun

supporting information, p. 30937 - 30942 (2021/11/19)

A straightforward aerobic oxidative esterification of aryl aldehydes with alcohols has been developed for the synthesis of substituted esters by employing vitamin B1 as a cost-effective, metal-free, and eco-friendly NHC catalyst. Air is used as a green terminal oxidant. The reaction is a useful addition to the existing NHC-catalytic oxidative esterification.

NOVEL CC-1065 ANALOGS AND THEIR CONJUGATES

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Page/Page column 148, (2010/06/17)

This invention relates to novel analogs of the DNA-alkylating agent CC-1065 and to their conjugates. Furthermore this invention concerns intermediates for the preparation of said agents and conjugates. The conjugates are designed to release their (multiple) payload after one or more activation steps and/or at a rate and time span controlled by the conjugate in order to selectively deliver and/or controllably release one or more of said DNA alkylating agents. The agents, conjugates, and intermediates can be used to treat an illness that is characterized by undesired (cell) proliferation. As an example, the agents and the conjugates of this invention may be used to treat a tumor.

QUINOXALINE DERIVATIVE

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Page/Page column 143, (2009/10/01)

The invention discloses quinoxaline derivatives or salts thereof having PDE9-inhibiting activity and being useful as treating agent of dysuria and the like, which are represented by the formula (I) in the formula, R1 and R2 each inde

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