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909119-73-9

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909119-73-9 Usage

General Description

4-Iodo-1-methoxy-2-(pentyloxy)benzene is an organic compound with the chemical formula C15H19IO2. It is a benzene derivative with an iodo and methoxy substituent at the 4 and 1 position, respectively, and a pentyloxy substituent at the 2 position. 4-Iodo-1-methoxy-2-(pentyloxy)benzene is commonly used in organic synthesis and pharmaceutical research as a building block for the synthesis of various pharmaceuticals and other organic compounds. It may also have potential applications in the development of new drugs due to its unique chemical structure and properties. However, it is important to handle this compound with caution due to its potential toxicity and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 909119-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,1,1 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 909119-73:
(8*9)+(7*0)+(6*9)+(5*1)+(4*1)+(3*9)+(2*7)+(1*3)=179
179 % 10 = 9
So 909119-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H17IO2/c1-3-4-5-8-15-12-9-10(13)6-7-11(12)14-2/h6-7,9H,3-5,8H2,1-2H3

909119-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-iodo-1-methoxy-2-pentoxybenzene

1.2 Other means of identification

Product number -
Other names 2-pentyloxy-5-iodoanisole

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:909119-73-9 SDS

909119-73-9Relevant articles and documents

Highly ordered columnar superlattice nanostructures with improved charge carrier mobility by thermotropic self-assembly of triphenylene-based discotics

Bi, Jingze,Wu, Hao,Zhang, Zhenhu,Zhang, Ao,Yang, Huanzhi,Feng, Yuwen,Fang, Yi,Zhang, Lina,Wang, Zhengran,Qu, Wentao,Liu, Feng,Zhang, Chunxiu

supporting information, p. 12463 - 12469 (2019/10/28)

A series of triphenylene esters with two ester groups at 2,3-, 2,7-, 2,6- and 3,6- substituent positions was successfully synthesized and fully investigated. Their self-assembly properties were exhaustively examined by DSC, POM, 1DXRD, 2DXRD, SAXS, TEM methods together with EDM and ESP calculations. It was unexpected that the 3,6-substituted triphenylene ester T5E36 formed an uncommonly helical hexagonal columnar superlattice structure made up of 91 right-handed helixes with a pitch of 60.3 ?. This helical superlattice structure was further studied by using transmission electron microscopy and the diameter of the T5E36 particles was found to be at the nanometer scale. Ultimately, the bipolar charge carrier mobility was measured by the time-of-flight method to be in the order of 10-1 cm2 V-1 s-1. The formation of this helical superlattice nanostructure no doubt improved their electronic properties and made them more attractive in organic electronics.

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