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4-[3-(1,3-benzodioxol-5-yl)propyl]phenol is a complex organic compound with the molecular formula C16H14O3. It is characterized by a phenol group (C6H5OH) attached to a propyl chain, which in turn is connected to a benzodioxole ring system. The benzodioxole ring, also known as dibenzo[b,d]oxepin, is a seven-membered aromatic ring with two oxygen atoms at positions 1 and 3. This specific arrangement of atoms and functional groups gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science. The compound's structure and properties make it a subject of interest for researchers studying the synthesis and applications of complex organic molecules.

40135-87-3

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40135-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40135-87-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,3 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40135-87:
(7*4)+(6*0)+(5*1)+(4*3)+(3*5)+(2*8)+(1*7)=83
83 % 10 = 3
So 40135-87-3 is a valid CAS Registry Number.

40135-87-3SDS

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 4-[3-(1,3-benzodioxol-5-yl)propyl]phenol

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:40135-87-3 SDS

40135-87-3Downstream Products

40135-87-3Relevant academic research and scientific papers

Biomimetic synthesis and anti-inflammatory effects of horsfiequinone A

Wang, Mei,Liu, Yuan-Lie,Li, Dashan,Xiao, Wen-Wen,Chen, Yang,Zhang, Hong-Lin,Zhan, Rui,Shao, Li-Dong

, (2021)

Inspired by the oxy-tyrosinase type II copper enzyme, a biomimetic synthesis of the natural product horsfiequinone A (1) has been achieved using CuOTf/DBED/O2 catalyzed oxidation as a key step. The synthetic route furnished 1 in 33% overall yield (64% brsm) from commercially available para-hydroxybenzaldehyde. Moreover, revisiting the biological activity of 1 resulted in the discovery of its in vitro inhibitory activity towards nitric oxide (NO) production in LPS-induced RAW264.7 cells with an IC50 value of 4.42 ± 0.81 μM. The anti-inflammatory effect of 1 was further supported by an iNOS expression inhibition assay and molecular docking simulation.

Synthesis and biological evaluation of chalcone, dihydrochalcone, and 1,3-diarylpropane analogs as anti-inflammatory agents

Vijaya Bhaskar Reddy, Mopur,Hung, Hsin-Yi,Kuo, Ping-Chung,Huang, Guan-Jhong,Chan, Yu-Yi,Huang, Shiow-Chyn,Wu, Shwu-Jen,Morris-Natschke, Susan L.,Lee, Kuo-Hsiung,Wu, Tian-Shung

, p. 1547 - 1550 (2017/03/17)

Twenty-one chalcones were prepared via aldol condensation and subsequent reduction of these compound led to the corresponding dihydrochalcone and 1,3-diphenylpropane derivatives. The synthetic products were examined for their effects on NO inhibition in L

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