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89280-77-3

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89280-77-3 Usage

General Description

4-Bromo-2,6-diiodoaniline is a chemical compound with the molecular formula C6H4BrI2NH2. It is a derivative of aniline, which is commonly used in the production of dyes and pharmaceuticals. This particular compound is a substituted aniline with bromine and iodine atoms attached to the benzene ring. It is a solid at room temperature and is typically handled and stored under strict safety precautions due to its potential for toxicity and reactivity. 4-Bromo-2,6-diiodoaniline may be used in organic synthesis, in the production of pharmaceuticals, and in research and development activities. It is important to handle and use this chemical with caution and in accordance with proper safety guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 89280-77-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,8 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89280-77:
(7*8)+(6*9)+(5*2)+(4*8)+(3*0)+(2*7)+(1*7)=173
173 % 10 = 3
So 89280-77-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H4BrI2N/c7-3-1-4(8)6(10)5(9)2-3/h1-2H,10H2

89280-77-3SDS

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-Bromo-2,6-diiodoaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,4-bromo-2,6-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:89280-77-3 SDS

89280-77-3Relevant articles and documents

Pyrrolo[3,2,1-kl]phenothiazine-based D-π-A type organic dyes for efficient dye-sensitized solar cells

Li, Feng,Zhu, Yi-Zhou,Zhang, Shao-Chun,Gao, Huan-Huan,Pan, Bin,Zheng, Jian-Yu

, p. 292 - 299 (2017)

Novel metal-free organic dyes based on polycyclic aromatic donor, pyrrolo[3,2,1-kl]phenothiazine, have been synthesized and applied in dye-sensitized solar cells. Combined with cyanoacrylic acid as the acceptor/anchoring group and simple π-spacers such as

Introducing High Density of Very Active Sites and Stepwise Postmodification for Tailoring the Porosity of Highly Demanding Cr3+-Based Metal-Organic Frameworks

Wang, Jun-Hao,Shi, Chun-Yang,Li, Meng-Na,Zhang, Ying,Niu, Jian-Chao,Zhang, Xian-Ming,Zhao, Ya-Wen,Li, Dan

supporting information, p. 12109 - 12115 (2021/08/20)

Chromium(III)-based metal-organic frameworks (Cr-MOFs) are highly robust and porous and have been very attractive in a wide range of investigations. However, the harsh direct synthetic conditions not only impede the synthesis of new Cr-MOFs but also restr

Approaches for Selective Synthesis of Ullazine Donor–Acceptor Systems

Drigo, Nikita A.,Paek, Sanghyun,Huckaba, Aron J.,Schouwink, Pascal A.,Tabet, Nouar,Nazeeruddin, Mohammad K.

supporting information, p. 17209 - 17212 (2017/11/27)

Methods for effective synthesis for the four possible isomeric 3,9-diphenylullazine carboxaldehydes and reactive halogen intermediates are described. Ullazine donor–acceptor (D–A) dyes were studied using UV/Vis, photoluminescence (PL) spectroscopy and cyclic voltammetry. X-ray single crystal diffraction analysis independently confirmed the structures of two key intermediates. A D–A dye based on ullazine with dihexylmalonate acceptor was tested as a dopant-free hole-transporting material (HTM) in a perovskite solar cell, exhibiting promising power conversion efficiency (PCE) reaching 13.07 %.

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