Welcome to LookChem.com Sign In|Join Free

CAS

  • or
(E)-3-(3-nitrophenyl)-1-(pyridin-2-yl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16232-04-5 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 16232-04-5 Structure
  • Basic information

    1. Product Name: (E)-3-(3-nitrophenyl)-1-(pyridin-2-yl)prop-2-en-1-one
    2. Synonyms:
    3. CAS NO:16232-04-5
    4. Molecular Formula:
    5. Molecular Weight: 254.245
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16232-04-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (E)-3-(3-nitrophenyl)-1-(pyridin-2-yl)prop-2-en-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-3-(3-nitrophenyl)-1-(pyridin-2-yl)prop-2-en-1-one(16232-04-5)
    11. EPA Substance Registry System: (E)-3-(3-nitrophenyl)-1-(pyridin-2-yl)prop-2-en-1-one(16232-04-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 16232-04-5(Hazardous Substances Data)

16232-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16232-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,3 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16232-04:
(7*1)+(6*6)+(5*2)+(4*3)+(3*2)+(2*0)+(1*4)=75
75 % 10 = 5
So 16232-04-5 is a valid CAS Registry Number.

16232-04-5Relevant articles and documents

Synthesis of azachalcones, their α-amylase, α-glucosidase inhibitory activities, kinetics, and molecular docking studies

Saleem, Faiza,Kanwal,Khan, Khalid Mohammed,Chigurupati, Sridevi,Solangi, Mehwish,Nemala, Appala Raju,Mushtaq, Maria,Ul-Haq, Zaheer,Taha, Muhammad,Perveen, Shahnaz

, (2020/12/09)

Diabetes being a chronic metabolic disorder have attracted the attention of medicinal chemists and biologists. The introduction of new and potential drug candidates for the cure and treatment of diabetes has become a major concern due to its increased pre

Coordination-driven self-assembly of anthraquinone-based metal-organic cages for photocatalytic selective [2 + 2] cycloaddition

Cui, Yong,Jiang, Hong,Jin, Yao,Liu, Yan,Tang, Xianhui,Zhang, Wenqiang

supporting information, p. 8533 - 8539 (2021/06/28)

Visible-light-promoted [2 + 2] cycloaddition provides a straightforward and efficient way to produce cyclobutanes, which are the core skeleton in commercial pharmaceuticals and fine chemicals. However, the control of the conformation to producesyn-head-to

Inhibitory potential of some chalcones on cathepsins B, H and L

Garg, Shweta,Raghav, Neera

, p. 72937 - 72949 (2015/09/15)

Cathepsins, intracellular proteases, are known to be involved in a number of physiological processes such as degradation of extracellular proteins, prohormone processing, progressions of atherosclerosis etc. High levels of cathepsins have also been indica

Synthesis and antibacterial activity of some heterocyclic chalcone analogues alone and in combination with antibiotics

Tran, Thanh-Dao,Nguyen, Thi-Thao-Nhu,Do, Tuong-Ha,Huynh, Thi-Ngoc-Phuong,Tran, Cat-Dong,Thai, Khac-Minh

experimental part, p. 6684 - 6696 (2012/08/28)

A series of simple heterocyclic chalcone analogues have been synthesized by Claisen Schmidt condensation reactions between substituted benzaldehydes and heteroaryl methyl ketones and evaluated for their antibacterial activity. The structures of the synthe

Efficient and Clean Aldol Condensation Catalyzed by Sodium Carbonate in Water

Zhang, Ze,Dong, Ya-Wei,Wang, Guan-Wu

, p. 966 - 967 (2007/10/03)

Efficient and environmentally friendly synthesis of chalcone and azachalcone was performed by aldol condensation of aldehydes with ketones in pure water catalyzed by sodium carbonate. In this convenient methodology, side reactions were avoided and thus high yields were achieved.

PHARMACEUTICAL USE OF TERPYRIDINE DERIVATIVE

-

, (2008/06/13)

A terpyridine derivative represented by general formula (I) (wherein R represents hydrogen, (un)substituted phenyl, pyridyl, etc.), which has the effect of promoting the production of nerve growth factors or a neurotrophic factor activity. Hence it can be

85. Development of Luminescent Europium(III) and Terbium(III) Chelates of 2,2':6',2''-Terpyridine Derivatives for Protein Labelling

Mukkala, Veli-Matti,Helenius, Matti,Hemmilae, Ilkka,Kankare, Jouko,Takalo, Harri

, p. 1361 - 1378 (2007/10/02)

The synthesis and luminescence properties are reported for 20 different chelates composed of 2,2':6',2''-terpyridine as the energy-absorbing and donating group, Eu(III) and Tb(III) as the emitting ions, methylenenitrilo(acetic acids) as the stable chelate

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 16232-04-5