Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Ethyl 3'-nitro-[1,1'-biphenyl]-4-carboxylate is a chemical compound characterized by the molecular formula C16H13NO4. It features a biphenyl backbone with a nitro group at the 3' position and an ethyl ester at the 4 position of the biphenyl ring. This nitro-substituted ester of biphenyl carboxylic acid is recognized for its potential in organic synthesis and pharmaceutical research, where it acts as a building block for the development of various drug molecules and organic materials. Its structure and properties have also led to the discovery of its biological and pharmacological activities, positioning it as a significant compound in the fields of medicinal chemistry and drug development.

108620-55-9

Post Buying Request

108620-55-9 Suppliers

Recommended suppliersmore

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

108620-55-9 Usage

Uses

Used in Organic Synthesis:
Ethyl 3'-nitro-[1,1'-biphenyl]-4-carboxylate is utilized as a key intermediate in organic synthesis for the creation of a variety of chemical compounds. Its unique structure allows for further functionalization and modification, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Ethyl 3'-nitro-[1,1'-biphenyl]-4-carboxylate serves as a precursor in the development of new drug molecules. Its presence in the molecular structure can influence the pharmacological properties of the final drug, contributing to its therapeutic effects and potential applications in medicine.
Used in Medicinal Chemistry:
Ethyl 3'-nitro-[1,1'-biphenyl]-4-carboxylate is employed as a building block in medicinal chemistry for the design and synthesis of bioactive compounds. Its incorporation into molecular frameworks can enhance the biological activity and selectivity of drug candidates, leading to the discovery of novel therapeutic agents.
Used in Drug Development:
In drug development, Ethyl 3'-nitro-[1,1'-biphenyl]-4-carboxylate is used as a starting material for the synthesis of potential drug candidates. Its versatile chemical properties enable the exploration of new chemical space and the optimization of drug-like properties, such as solubility, stability, and bioavailability.
Used in Chemical Industry:
Ethyl 3'-nitro-[1,1'-biphenyl]-4-carboxylate finds applications in the chemical industry for the production of various organic materials and specialty chemicals. Its unique structure and reactivity contribute to the development of new materials with specific properties and applications in areas such as coatings, polymers, and advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 108620-55-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,6,2 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 108620-55:
(8*1)+(7*0)+(6*8)+(5*6)+(4*2)+(3*0)+(2*5)+(1*5)=109
109 % 10 = 9
So 108620-55-9 is a valid CAS Registry Number.

108620-55-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 3'-nitro-[1,1'-biphenyl]-4-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 4-(3-nitrophenyl)benzoate

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:108620-55-9 SDS

108620-55-9Downstream Products

108620-55-9Relevant articles and documents

METHOD OF TREATMENT AND DEVICE

-

Paragraph 0046; 0054, (2020/07/25)

A method and an angioplasty balloon catheter used in a method of preventing or minimizing incidence of neointimal hyperplasia (NIH) in a blood vessel of an animal following angioplasty treatment. The method comprising locating the angioplasty balloon cath

Suzuki-Miyaura reaction catalyzed by graphene oxide supported palladium nanoparticles

Shang, Ningzhao,Feng, Cheng,Zhang, Haiyan,Gao, Shutao,Tang, Ranxiao,Wang, Chun,Wang, Zhi

, p. 111 - 115 (2013/07/26)

Pd supported on polyamine modified graphene oxide (GO-NH 2-Pd2 +) was fabricated for the first time. The prepared catalyst was characterized by transmission electron microscopy, X-ray diffraction spectroscopy, X-ray photoelectron spectroscopy and infrared spectroscopy. The catalytic activity of the prepared catalyst was investigated by employing Suzuki-Miyaura coupling reaction as a model reaction. A series of biphenyl compounds were synthesized through the Suzuki-Miyaura reaction using GO-NH2-Pd2 + as catalyst. The yields of the products were in the range from 71% to 95%. The catalyst can be readily recovered and reused at least 10 consecutive cycles without significant loss its catalytic activity.

Conformational analogues of Oxamflatin as histone deacetylase inhibitors

Dear, Anthony E.,Liu, Hong B.,Mayes, Penelope A.,Perlmutter, Patrick

, p. 3778 - 3784 (2008/09/18)

Conformational analogues of the hydroxamic acid Oxamflatin 1 - compounds 3a, 3b and 4 - have been synthesised to enable evaluation of the impact of varying the linking section on histone deacetylase inhibition. Preliminary testing indicates treatment of l

Derivatives of aminobenzoic and aminobiphenylcarboxylic acids useful as anti-cancer agents

-

, (2008/06/13)

The present invention provides compounds having the formula: wherein n is0or1; R is —NH2or wherein R1and R2are independently selected from the group consisting of H, alkyl, aralkyl, heteroaralkyl, carboxy, carboxyalkyl, and carbamoyl; Q is R3C(O)— or wherein R5is selected from the group consisting of H, alkyl, aralkyl, heteroaralkyl, and carbamoylalkyl, and R3and R4are selected from the group consisting of H, alkyl, alkoxy, arylalkoxy, aralkyl, heteroaralkyl, and carbamoylalkyl; the Q—NH—(CH2)n— and the —C(O)R substituents of the compound of formula I are independently positioned ortho, meta, orpara relative to the carbon atoms that form the bond between the two phenyl groups to which said substituents are bound, with the proviso that said substituents are not both positioned ortho; and the Q—NH—(CH2)nand the —C(O)R substituents of the compound of formula II are positioned meta orpara to each other; or a biolabile ester thereof, or a pharmaceutically acceptable salt thereof. The compounds are useful for treating uPA- or uPAR-mediated disorders, e.g., tumor metastasis, tumor angiogenesis, restenosis, chronic inflammation, or corneal angiogenesis.

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 108620-55-9