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2-Propen-1-one, 1-benzo[b]thien-2-yl-3-phenyl-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93486-61-4

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93486-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93486-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,8 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 93486-61:
(7*9)+(6*3)+(5*4)+(4*8)+(3*6)+(2*6)+(1*1)=164
164 % 10 = 4
So 93486-61-4 is a valid CAS Registry Number.

93486-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1-benzothiophen-2-yl)-3-phenylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names -

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:93486-61-4 SDS

93486-61-4Relevant academic research and scientific papers

New zileuton-hydroxycinnamic acid hybrids: Synthesis and structure-activity relationship towards 5-lipoxygenase inhibition

Chiasson, Audrey Isabel,Robichaud, Samuel,Ndongou Moutombi, Fanta J.,Hébert, Mathieu P.A.,Mbarik, Maroua,Surette, Marc E.,Touaibia, Mohamed

, (2020/10/29)

A novel series of zileuton-hydroxycinnamic acid hybrids were synthesized and screened as 5-lipoxygenase (5-LO) inhibitors in stimulated HEK293 cells and polymorphonuclear leukocytes (PMNL). Zileuton’s (1) benzo[b]thiophene and hydroxyurea subunits combine

Highly Enantioselective Epoxidation of α,β-Unsaturated Ketones Using Amide-Based Cinchona Alkaloids as Hybrid Phase-Transfer Catalysts

Jurczak, Janusz,Majdecki, Maciej,Tyszka-Gumkowska, Agata

supporting information, (2020/11/13)

A series of 20 one chiral epoxides were obtained with excellent yields (up to 99%) and enantioselectivities (up to >99% ee) using hybrid amide-based Cinchona alkaloids. Our method is characterized by low catalyst loading (0.5 mol %) and short reaction times. Moreover, the epoxidation process can be carried out in 10 cycles, without further catalyst addition to the reaction mixture. This methodology significantly enhance the scale of the process using very low catalyst loading.

Substituted benzothiophene or benzofuran derivatives as a novel class of bone morphogenetic protein-2 up-Regulators: Synthesis, structure-activity relationships, and preventive bone loss efficacies in senescence accelerated mice (SAMP6) and ovariectomized

Guo, Hui-Fang,Shao, Hua-Yi,Yang, Zhao-Yong,Xue, Si-Tu,Li, Xue,Liu, Zong-Ying,He, Xiao-Bo,Jiang, Jian-Dong,Zhang, Yue-Qin,Si, Shu-Yi,Li, Zhuo-Rong

experimental part, p. 1819 - 1829 (2010/08/20)

In this work, substituted benzothiophene and benzofuran compounds were found to be a new class of potential anabolic agents by enhancing BMP-2 expression. A series of benzothiophene and benzofuran derivatives have been synthesized, and their activities of

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