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153033-34-2

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153033-34-2 Usage

General Description

The chemical 1,4-DIIODO-2,5-BIS(DECYLOXY)BENZENE is a compound with the molecular formula C26H42I2O2. It is also known as decyloxy-bis(2,5-diiodophenyl) or dibenzo[d]iodooxane. This chemical is a white to off-white crystalline powder that is sparingly soluble in water and soluble in organic solvents. It is primarily used as a precursor in the synthesis of electronic materials, such as organic semiconductors and conductive polymers. It is also used as a reagent in organic synthesis and as an intermediate in pharmaceutical research. This chemical is often handled and used in laboratory settings with proper safety precautions due to its potential hazards if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 153033-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,0,3 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 153033-34:
(8*1)+(7*5)+(6*3)+(5*0)+(4*3)+(3*3)+(2*3)+(1*4)=92
92 % 10 = 2
So 153033-34-2 is a valid CAS Registry Number.

153033-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-didecoxy-2,5-diiodobenzene

1.2 Other means of identification

Product number -
Other names Benzene,1,4-bis(decyloxy)-2,5-diiodo

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:153033-34-2 SDS

153033-34-2Relevant articles and documents

Synthesis, spectroscopic and nonlinear optical properties of multiple [60]fullerene-oligo(p-phenylene ethynylene) hybrids

Zhao, Yuming,Shirai, Yasuhiro,Slepkov, Aaron D.,Cheng, Long,Alemany, Lawrence B.,Sasaki, Takashi,Hegmann, Frank A.,Tour, James M.

, p. 3643 - 3658 (2007/10/03)

A series of multiple [60]fullerene terminated oligo(p-phenylene ethynylene) (OPE) hybrid compounds has been synthesized through a newly developed in situ ethynylation method. Structural and magnetic shielding properties of the highly unsaturated carbon-ri

Facile synthesis of multifullerene-OPE hybrids via in situ ethynylation

Shirai, Yasuhiro,Zhao, Yuming,Cheng, Long,Tour, James M.

, p. 2129 - 2132 (2007/10/03)

A series of fullerene-terminated oligo(phenylene ethynylene)s (OPEs) (1a-d and 2) have been synthesized and further characterized by cyclic voltammetry (CV) and UV-vis spectroscopy. The key step in the syntheses is an effective one-pot reaction that allow

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