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3164-07-6

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3164-07-6 Usage

General Description

4-(Benzo[d]oxazol-2-yl)-2-Methoxyphenol is a chemical compound with the molecular formula C14H11NO3. It is a synthetic compound that belongs to the oxazole family and contains a phenol group and a methoxy group. 4-(Benzo[d]oxazol-2-yl)-2-Methoxyphenol is used in the pharmaceutical industry for its potential therapeutic properties, including anti-inflammatory and antioxidant effects. It has also been studied for its potential use in the development of new drugs for various medical conditions. Additionally, it has been investigated for its potential use in materials science, such as in the development of new polymers and as a fluorescent dye for biological imaging applications.

Check Digit Verification of cas no

The CAS Registry Mumber 3164-07-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,6 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3164-07:
(6*3)+(5*1)+(4*6)+(3*4)+(2*0)+(1*7)=66
66 % 10 = 6
So 3164-07-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H11NO3/c1-17-13-8-9(6-7-11(13)16)14-15-10-4-2-3-5-12(10)18-14/h2-8,16H,1H3

3164-07-6SDS

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 4-(1,3-Benzoxazol-2-yl)-2-methoxyphenol

1.2 Other means of identification

Product number -
Other names 4-(1,3-benzothiazole-2-yl)-2-bromoaniline

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:3164-07-6 SDS

3164-07-6Relevant articles and documents

Facile one-pot synthesis of (benzoxazol-2'-yl)bicyclo[2.2.2]octen-2-one derivatives

Naganaboina, Ram Tilak,Peddinti, Rama Krishna

, p. 6245 - 6253 (2015)

Abstract A simple and efficient one-pot synthesis of 5-(benzoxazol-2'-yl)bicyclo[2.2.2]octen-2-one derivatives from readily accessible starting materials has been demonstrated. The current protocol involves diacetoxyiodobenzene mediated domino oxidative c

Synthesis, DNA-binding ability and anticancer activity of benzothiazole/benzoxazole-pyrrolo[2,1-c][1,4]benzodiazepine conjugates

Kamal, Ahmed,Reddy, K. Srinivasa,Khan, M. Naseer A.,Shetti, Rajesh V.C.R.N.C.,Ramaiah, M. Janaki,Pushpavalli,Srinivas, Chatla,Pal-Bhadra, Manika,Chourasia, Mukesh,Sastry, G. Narahari,Juvekar, Aarti,Zingde, Surekha,Barkume, Madan

experimental part, p. 4747 - 4761 (2010/08/20)

A series of benzothiazole and benzoxazole linked pyrrolobenzodiazepine conjugates attached through different alkane or alkylamide spacers was prepared. Their anticancer activity, DNA thermal denaturation studies, restriction endonuclease digestion assay and flow cytometric analysis in human melanoma cell line (A375) were investigated. One of the compounds of the series 17d showed significant anticancer activity with promising DNA-binding ability and apoptosis caused G0/G1 phase arrest at sub-micromolar concentrations. To ascertain the binding mode and understand the structural requirement of DNA binding interaction, molecular docking studies using gold program and more rigorous 2 ns molecular dynamic simulations using Molecular Mechanics-Poisson-Boltzman Surface Area (MM-PBSA) approach including the explicit solvent were carried out. Further, the compound 17d was evaluated for in vivo efficacy studies in human colon cancer HT29 xenograft mice.

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