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2-Propenamide, N-butyl-3-(3,4-dihydroxyphenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136944-13-3

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136944-13-3 Usage

Physical State

White solid

Melting Point

84-87 degrees Celsius

Solubility

Soluble in organic solvents

Common Uses

Production of personal care and cosmetic products

Biological Activities

Potential antioxidant and anti-inflammatory properties

Pharmaceutical Applications

Under study for potential use in pharmaceuticals

Health Hazards

Requires careful handling due to potential health hazards

Environmental Impact

Needs to be managed responsibly to mitigate environmental impacts

Check Digit Verification of cas no

The CAS Registry Mumber 136944-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,9,4 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 136944-13:
(8*1)+(7*3)+(6*6)+(5*9)+(4*4)+(3*4)+(2*1)+(1*3)=143
143 % 10 = 3
So 136944-13-3 is a valid CAS Registry Number.

136944-13-3Downstream Products

136944-13-3Relevant academic research and scientific papers

Derivatives of caffeic acid, a natural antioxidant, as the basis for the discovery of novel nonpeptidic neurotrophic agents

Moosavi, Fatemeh,Hosseini, Razieh,Rajaian, Hamid,Silva, Tiago,Magalh?es e Silva, Diogo,Saso, Luciano,Edraki, Najmeh,Miri, Ramin,Borges, Fernanda,Firuzi, Omidreza

, p. 3235 - 3246 (2017)

Neurodegenerative disorders, such as Parkinson's disease and Alzheimer's disease, threaten the lives of millions of people and the number of affected patients is constantly growing with the increase of the aging population. Small molecule neurotrophic age

Optimization of physicochemical properties is a strategy to improve drug-likeness associated with activity: Novel active and selective compounds against Trypanosoma cruzi

Amaral, Maiara,Romanelli, Maiara M.,Tempone, Andre G.,Varela, Marina T.,de Castro Levatti, Erica V.,Fernandes, Jo?o Paulo S.

, (2022/01/31)

Trypanosoma cruzi is the causing agent of Chagas disease, a parasitic infection without efficient treatment for chronic patients. Despite the efforts, no new drugs have been approved for this disease in the last 60 years. Molecular modifications based on

Bio-inspired benzo[k,l]xanthene lignans: Synthesis, DNA-interaction and antiproliferative properties

Spatafora, Carmela,Barresi, Vincenza,Bhusainahalli, Vedamurthy M.,Di Micco, Simone,Musso, Nicolo,Riccio, Raffaele,Bifulco, Giuseppe,Condorelli, Daniele,Tringali, Corrado

, p. 2686 - 2701 (2014/05/06)

In this work twelve benzo[k,l]xanthene lignans were synthesized by biomimetic, Mn-mediated oxidative coupling of caffeic esters and amides. These compounds, bearing different flexible pendants at position C1/C2 of the aromatic core, interact with DNA in a dual mode, as confirmed by DF-STD NMR analysis and molecular docking: the planar core acts as a base pair intercalant, whereas the flexible pendants act as minor groove binders. Their antiproliferative activity was evaluated on a panel of six tumor cell lines: HT-29, Caco-2, HCT-116 (human colon carcinoma), H226, A549 (human lung carcinoma), and SH-SY5Y (human neuroblastoma). All compounds under study, except 29, resulted in activity against one or more cell lines, and the markedly lipophilic esters 13 and 28 showed the highest activity. Compound 13 was more active than the anticancer drug 5-fluorouracil (5-FU) towards HCT-116 (colon, GI50 = 3.16 μM) and H226 (lung, GI50 = 4.33 μM) cell lines. This journal is the Partner Organisations 2014.

Simple amidation of unprotected phenol-containing 2-alkenoic acids

Morais, Goreti Ribeiro,Watanabe, Masataka,Tanaka, Yasuko,Thiemann, Thies

, p. 802 - 807 (2007/10/03)

A series of amides of 2-E-alkenoic acids have been synthesised through the activation of these acids with dicyclohexylcarbodiimide / pentafluorophenol and further reaction with amines under microwave irradiation. In daylight, the E-configured amides under

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