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755027-18-0

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755027-18-0 Usage

General Description

2-Bromo-5-iodoanisole is a chemical compound with the molecular formula C7H6BrIO. It is a derivative of anisole, a methoxybenzene, with bromine and iodine substituents. 2-Bromo-5-iodoanisole is mainly used as a reagent in organic synthesis and as an intermediate for the production of various pharmaceuticals, agrochemicals, and other fine chemicals. 2-Bromo-5-iodoanisole is also used in the preparation of advanced materials and in research and development in the field of organic chemistry. Its specific properties and applications make it a useful and versatile chemical in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 755027-18-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,5,0,2 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 755027-18:
(8*7)+(7*5)+(6*5)+(5*0)+(4*2)+(3*7)+(2*1)+(1*8)=160
160 % 10 = 0
So 755027-18-0 is a valid CAS Registry Number.

755027-18-0SDS

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 1-bromo-4-iodo-2-methoxybenzene

1.2 Other means of identification

Product number -
Other names BENZENE,1-BROMO-4-IODO-2-METHOXY

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:755027-18-0 SDS

755027-18-0Relevant articles and documents

Using Nature's polyenes as templates: studies of synthetic xanthomonadin analogues and realising their potential as antioxidants

Madden, Katrina S.,Jokhoo, Hans R. E.,Conradi, Fabian D.,Knowles, Jonathan P.,Mullineaux, Conrad W.,Whiting, Andrew

supporting information, p. 3752 - 3759 (2019/04/17)

Two truncated analogues of the polyenyl photoprotective xanthomonadin pigments have been synthesised utilising an iterative Heck-Mizoroki (HM)/iododeboronation cross coupling approach and investigated as models of the natural product photoprotective agent

Active Molybdenum-Based Anode for Dehydrogenative Coupling Reactions

Beil, Sebastian B.,Müller, Timo,Sillart, Sydney B.,Franzmann, Peter,Bomm, Alexander,Holtkamp, Michael,Karst, Uwe,Schade, Wolfgang,Waldvogel, Siegfried R.

supporting information, p. 2450 - 2454 (2018/02/09)

A new and powerful active anode system that can be operated in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) has been discovered. In HFIP the molybdenum anode forms a compact, conductive, and electroactive layer of higher-valent molybdenum species. This system can replace powerful but stoichiometrically required MoV reagents for the dehydrogenative coupling of aryls. This electrolytic reaction is more sustainable and allows the conversion of a broad scope of activated arenes.

Progress Toward a Semi-Synthetic Organism with an Unrestricted Expanded Genetic Alphabet

Dien, Vivian T.,Holcomb, Matthew,Feldman, Aaron W.,Fischer, Emil C.,Dwyer, Tammy J.,Romesberg, Floyd E.

supporting information, p. 16115 - 16123 (2018/11/23)

We have developed a family of unnatural base pairs (UBPs), exemplified by the pair formed between dNaM and dTPT3, for which pairing is mediated not by complementary hydrogen bonding but by hydrophobic and packing forces. These UBPs enabled the creation of

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