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1-(2-methoxynaphthalen-1-yl)-3-phenylprop-2-en-1-one, also known as 2-Methoxy-1-naphthyl-3-phenyl-2-propen-1-one, is a chemical compound with a molecular formula C19H16O2. It is a yellow to orange crystalline powder that exhibits a slightly sweet, floral, and spicy odor.

4487-15-4

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4487-15-4 Usage

Uses

Used in Fragrance Industry:
1-(2-methoxynaphthalen-1-yl)-3-phenylprop-2-en-1-one is used as a fragrance ingredient for its sweet, floral, and spicy scent. It is incorporated into perfumes, soaps, and other personal care products to provide a pleasant aroma.
Used in Skincare Industry:
This chemical is used as an antimicrobial and antioxidant agent in the formulation of skincare products. Its properties help to protect the skin from harmful microorganisms and oxidative stress, promoting healthier and more resilient skin.
However, it is crucial to handle 1-(2-methoxynaphthalen-1-yl)-3-phenylprop-2-en-1-one with care, as it can cause skin and eye irritation and is harmful if ingested. Proper safety measures should be taken during its use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 4487-15-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,8 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4487-15:
(6*4)+(5*4)+(4*8)+(3*7)+(2*1)+(1*5)=104
104 % 10 = 4
So 4487-15-4 is a valid CAS Registry Number.

4487-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name benzylidine-2-methoxy-5,6-benzoacetophenone

1.2 Other means of identification

Product number -
Other names 2-Methoxy-1-cinnamoyl-naphthalin

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:4487-15-4 SDS

4487-15-4Relevant academic research and scientific papers

Synthesis, biological evaluation, and molecular modelling of new naphthalene-chalcone derivatives as potential anticancer agents on MCF-7 breast cancer cells by targeting tubulin colchicine binding site

Wang, Guangcheng,Liu, Wenjing,Gong, Zipeng,Huang, Yong,Li, Yongjun,Peng, Zhiyun

, p. 139 - 144 (2020)

A series of naphthalene-chalcone derivatives (3a–3t) were prepared and evaluated as tubulin polymerisation inhibitor for the treatment of breast cancer. All compounds were evaluated for their antiproliferative activity against MCF-7 cell line. The most of compounds displayed potent antiproliferative activity. Among them, compound 3a displayed the most potent antiproliferative activity with an IC50 value of 1.42 ± 0.15 μM, as compared to cisplatin (IC50 = 15.24 ± 1.27 μM). Additionally, the promising compound 3a demonstrated relatively lower cytotoxicity on normal cell line (HEK293) compared to tumour cell line. Furthermore, compound 3a was found to induce significant cell cycle arrest at the G2/M phase and cell apoptosis. Compound 3a displayed potent tubulin polymerisation inhibitory activity with an IC50 value of 8.4 μM, which was slightly more active than the reference compound colchicine (IC50 = 10.6 μM). Molecular docking analysis suggested that 3a interact and bind at the colchicine binding site of the tubulin.

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