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Benzenamine, 4-fluoro-2,6-diiodo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88162-54-3

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88162-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88162-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,1,6 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88162-54:
(7*8)+(6*8)+(5*1)+(4*6)+(3*2)+(2*5)+(1*4)=153
153 % 10 = 3
So 88162-54-3 is a valid CAS Registry Number.

88162-54-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluoro-2,6-diiodoaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,4-fluoro-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:88162-54-3 SDS

88162-54-3Upstream product

88162-54-3Relevant academic research and scientific papers

One-Pot Synthesis of Pyrrolo[3,2,1-kl]phenothiazines through Copper-Catalyzed Tandem Coupling/Double Cyclization Reaction

Tang, Jiaming,Xu, Bingqing,Mao, Xi,Yang, Hongyan,Wang, Xiaoxia,Lv, Xin

, p. 11108 - 11114 (2015)

A novel and efficient synthesis of pyrrolo[3,2,1-kl]phenothiazines has been developed through a Cu(I)-catalyzed tandem C-S coupling/double cyclization process. Using 2-alkynyl-6-iodoanilines and o-bromobenzenethiols as the starting materials, a wide range

A mild and convenient synthesis of 1,2,3-triiodoarenes via consecutive iodination/diazotization/iodination strategy

Al-Zoubi, Raed M.,Futouh, Hassan Abul,McDonald, Robert

, p. 1570 - 1575 (2014/01/23)

A mild and convenient synthesis of 1,2,3-triiodoarenes has been developed. This method consists of two steps which can be performed on multigram scale with moderate to excellent yields. This report discloses a practical synthesis of 1,2,3-triiodoarenes and 1,2,3-trihaloarenes that is general in scope, operationally simple, scalable, and is easy to workup and to purify. We also report the first regioselective transmetalation reaction of 1,2,3-triiodoarenes to provide ortho-diiodoaryl derivatives, which are useful building blocks and indeed are hard to make by other means. CSIRO 2013.

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