Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Ethyl 4-Bromo-2-fluorobenzoate is a specialized chemical compound with the molecular formula C9H8BrFO2. It belongs to the category of benzoates, which are organic compounds containing a -C(O)OC6H5 group. Ethyl 4-BroMo-2-fluorobenzoate features a benzene ring as its core structure, with additional bromine and fluorine atoms, making it a halogenated benzoate. Ethyl 4-Bromo-2-fluorobenzoate is typically synthesized in a laboratory setting and is known for its high reactivity due to the presence of halogen atoms.

474709-71-2

Post Buying Request

474709-71-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

474709-71-2 Usage

Uses

Used in Chemical Synthesis:
Ethyl 4-Bromo-2-fluorobenzoate is used as a key intermediate in the synthesis of various other chemical compounds. Its reactivity, stemming from the halogen atoms, makes it a valuable component in creating a wide range of products.
Used in Chemical Reactions:
Ethyl 4-Bromo-2-fluorobenzoate is employed as a halogenating and esterifying agent in different chemical reactions. Its role in these processes is crucial for the production of specific compounds and materials.
Used in Pharmaceutical Industry:
Ethyl 4-Bromo-2-fluorobenzoate is used as a building block in the development of pharmaceutical compounds. Its unique structure and reactivity contribute to the creation of new drugs and therapeutic agents.
Used in Research and Development:
Ethyl 4-Bromo-2-fluorobenzoate is utilized in research settings to explore its potential applications and properties. Its presence in various chemical reactions and syntheses provides valuable insights into the development of new materials and compounds.
It is important to handle Ethyl 4-Bromo-2-fluorobenzoate with care due to potential health and environmental hazards associated with it. Proper safety measures should be taken to minimize risks during its synthesis and use.

Check Digit Verification of cas no

The CAS Registry Mumber 474709-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,7,0 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 474709-71:
(8*4)+(7*7)+(6*4)+(5*7)+(4*0)+(3*9)+(2*7)+(1*1)=182
182 % 10 = 2
So 474709-71-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H8BrFO2/c1-2-13-9(12)7-4-3-6(10)5-8(7)11/h3-5H,2H2,1H3

474709-71-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-bromo-2-fluorobenzoate

1.2 Other means of identification

Product number -
Other names 4-bromo-2-fluorophenyl ethyl carbonate

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:474709-71-2 SDS

474709-71-2Relevant articles and documents

Highly selective electroreductive linear dimerization of electron-deficient vinylarenes

Ning, Shulin,Zheng, Lianyou,Bai, Ya,Wang, Shutao,Wang, Siyu,Shi, Lingling,Gao, Qiansong,Che, Xin,Zhang, Zhuoqi,Xiang, Jinbao

supporting information, (2021/11/16)

A direct electroreductive dimerization of electron-deficient vinylarenes for the synthesis of 1,4-diarylbutane has been developed using a simple undivided cell with inexpensive carbon electrodes at room temperature. The control and deuterium-labeling experiments of electroreductive dimerization suggest that the hydrogen source comes from the solvent CH3CN. This protocol provides a mild and efficient route for the construction of C–C bond in moderate to good yields with high regioselectivity and broad substrate scope.

Synthesis and bioactivity of sulfide derivatives containing 1,3,4-oxadiazole and pyridine

Yu, Gang,Chen, Shunhong,He, Feng,Luo, Dexia,Zhang, Yu,Wu, Jian

, p. 1075 - 1085 (2019/09/10)

A series of novel sulfide derivatives containing 1,3,4-oxadiazole and pyridine were synthesized, characterized, and tested for their antibacterial activity against tobacco bacterial wilt and rice bacterial blight and for insecticidal activity toward diamondback moth. The results showed that some compounds had good insecticidal and bactericidal activity, e.g., the activities of compounds 6e and 6g–6j toward tobacco bacterial wilt were much better than those of commercial thiodiazole-copper, and some of the synthesized compounds possessed good insecticidal activity against Plutella xylostella. Compounds 6d, 6h, 6j, 6l, 6p, 6r, and 6p displayed over 93% activity at 500 mg L? 1.

Design, synthesis, insecticidal activity and 3D-QSR study for novel trifluoromethyl pyridine derivatives containing an 1,3,4-oxadiazole moiety

Xu,Wang,Luo,Yu,Guo,Fu,Zhao,Wu

, p. 6306 - 6314 (2018/02/19)

A series of trifluoromethyl pyridine derivatives containing 1,3,4-oxadiazole moiety was designed, synthesized and bio-assayed for their insecticidal activity. The result of bio-assays indicated the synthesized compounds exhibited good insecticidal activity against Mythimna separata and Plutella xylostella, most of the title compounds show 100% insecticidal activity at 500 mg L-1 and >80% activity at 250 mg L-1 against the two pests. Compounds E18 and E27 showed LC50 values of 38.5 and 30.8 mg L-1 against Mythimna separata, respectively, which were close to that of avermectin (29.6 mg L-1); compounds E5, E6, E9, E10, E15, E25, E26, and E27 showed 100% activity at 250 mg L-1, which were better than chlorpyrifos (87%). CoMFA and CoMSIA models with good predictability were proposed, which revealed the electron-withdrawing groups with an appropriate bulk at 2- and 4-positions of benzene ring could enhance insecticidal activity.

Discovery of Highly Potent Liver X Receptor β Agonists

Kick, Ellen K.,Busch, Brett B.,Martin, Richard,Stevens, William C.,Bollu, Venkataiah,Xie, Yinong,Boren, Brant C.,Nyman, Michael C.,Nanao, Max H.,Nguyen, Lam,Plonowski, Artur,Schulman, Ira G.,Yan, Grace,Zhang, Huiping,Hou, Xiaoping,Valente, Meriah N.,Narayanan, Rangaraj,Behnia, Kamelia,Rodrigues, A. David,Brock, Barry,Smalley, James,Cantor, Glenn H.,Lupisella, John,Sleph, Paul,Grimm, Denise,Ostrowski, Jacek,Wexler, Ruth R.,Kirchgessner, Todd,Mohan, Raju

supporting information, p. 1207 - 1212 (2016/12/18)

Introducing a uniquely substituted phenyl sulfone into a series of biphenyl imidazole liver X receptor (LXR) agonists afforded a dramatic potency improvement for induction of ATP binding cassette transporters, ABCA1 and ABCG1, in human whole blood. The ag

2-Substituted-oxy-5-methylsulfonyl pyridine piperazine acidamide analogue and preparation method and application thereof

-

Paragraph 0176; 0177, (2016/10/08)

The invention discloses 2-substituted-oxy-5-methylsulfonyl pyridine piperazine acidamide analogue and a preparation method and application thereof, and particularly, relates to 2-substituted-oxy-5-methylsulfonyl pyridine piperazine acidamide analogue with

HETEROCYCLIC COMPOUND

-

Paragraph 0880, (2015/04/15)

The present invention provides a compound having a superior JAK inhibitory action, which is useful as an agent for the prophylaxis or treatment of autoimmune diseases (rheumatoid arthritis, psoriasis, inflammatory bowel disease, Sjogren's syndrome, Behcet's disease, multiple sclerosis, systemic lupus erythematosus, etc.), cancer (leukemia, uterine leiomyosarcoma, prostate cancer, multiple myeloma, cachexia, myelofibrosis, etc.) and the like, or a salt thereof. The present invention relates to a compound represented by the formula wherein each symbol is as defined in the specification, or a salt thereof.

Pesticidal compositions and processes related thereto

-

Page/Page column 53; 54, (2016/01/09)

This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

-

Paragraph 0258; 0259; 0265; 0266, (2015/12/30)

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such molecules and intermediates used in such processes, compositions containing such molecules, and processes of using such molecules against such pests. These molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses molecules having the following formula (“Formula One”).

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

-

Page/Page column 53; 54, (2014/07/08)

This document discloses molecules having the following formula ("Formula One"): and processes associated therewith.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

-

Paragraph 0244-0245, (2014/06/25)

This document discloses molecules having the following formula (“Formula One”): and processes associated therewith.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 474709-71-2