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51560-25-9

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51560-25-9 Usage

Structure

Benzene ring with two methoxy groups (-OCH3) and two iodine atoms (-I) attached to adjacent carbon atoms

Type

Chemical compound

Derivative

DIODO derivative of dimethoxybenzene

Applications

a. Building block in the synthesis of various organic compounds
b. Used in pharmaceuticals and agrochemicals
c. Employed in materials science
d. Utilized as a reagent in chemical research

Health hazards

Potential health risks associated with improper handling

Environmental impact

Possible negative effects on the environment if not disposed of properly

Safety precautions

Proper handling and disposal procedures should be followed when working with 1,4-DIIODO-2,3-DIMETHOXYBENZENE

Check Digit Verification of cas no

The CAS Registry Mumber 51560-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,6 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51560-25:
(7*5)+(6*1)+(5*5)+(4*6)+(3*0)+(2*2)+(1*5)=99
99 % 10 = 9
So 51560-25-9 is a valid CAS Registry Number.

51560-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-diiodo-2,3-dimethoxybenzene

1.2 Other means of identification

Product number -
Other names Benzene,1,4-diiodo-2,3-dimethoxy

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:51560-25-9 SDS

51560-25-9Relevant articles and documents

A rings-in-pores net: Crown ether-based covalent organic frameworks for phase-transfer catalysis

Guo, Wen-Di,Hu, Bingwen,Jiang, Wei-Ling,Lou, Xiaobing,Ma, De-Li,Qi, Qiao-Yan,Shen, Ji-Chuang,Shen, Ming,Yang, Hai-Bo,Zhao, Xin

supporting information, p. 595 - 598 (2020/01/29)

We herein present a new family of crown ether-based covalent organic frameworks (CE-COFs) for the first time. The CE-COFs show excellent phase-transfer catalytic performance in various nucleophilic substitution reactions.

SPIRO RING COMPOUND AS HEPATITIS C VIRUS (HCV) INHIBITOR AND USES THEREOF FIELD OF THE INVENTION

-

Page/Page column 155; 156; 157, (2014/06/23)

A compound of formula (I) or a stereoisomer, a geometric isomer. a tautomer, an N-oxide, a hydrate, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof is provided, which can be used for treating HCV infection or a HCV disorder. Also a pharmaceutical composition comprising the compound and the use of the compound and the pharmaceutical composition thereof are provided, which can also be used for treating HCV infection or a HCV disorder.

Catechol-based macrocyclic rods: En route to redox-active molecular switches

Weibel, Nicolas,Mishchenko, Artera,Wandlowski, Thomas,Neuburger, Markus,Leroux, Yann,Mayor, Marcel

scheme or table, p. 6140 - 6150 (2010/03/24)

The design and synthesis of the macrocyclic turnstile 1 comprising a terminally sulfur-functionalized molecular rod and a redox-active catechol subunit is described, The shape-persistent macrocyclic scaffold consists of alternating arylene and ethynylene

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