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1416549-07-9

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1416549-07-9 Usage

General Description

2-Fluoro-5-iodo-1,3-dimethylbenzene is a chemical compound with the molecular formula C8H8FIL. It is an organic compound that contains both fluorine and iodine atoms attached to a benzene ring. 2-Fuoro-5-iodo-1,3-dimethylbenzene is used in the production of pharmaceuticals, agrochemicals, and other organic synthesis processes. It is also used as an intermediate in the synthesis of various other chemicals. 2-Fluoro-5-iodo-1,3-dimethylbenzene is primarily known for its aromatic properties and its use in organic chemistry research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 1416549-07-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,6,5,4 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1416549-07:
(9*1)+(8*4)+(7*1)+(6*6)+(5*5)+(4*4)+(3*9)+(2*0)+(1*7)=159
159 % 10 = 9
So 1416549-07-9 is a valid CAS Registry Number.

1416549-07-9SDS

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 2-fluoro-5-iodo-1,3-dimethylbenzene

1.2 Other means of identification

Product number -
Other names -

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:1416549-07-9 SDS

1416549-07-9Downstream Products

1416549-07-9Relevant articles and documents

Sterically controlled iodination of arenes via iridium-catalyzed C-H borylation

Partridge, Benjamin M.,Hartwig, John F.

supporting information, p. 140 - 143 (2013/03/28)

A mild method to prepare aryl and heteroaryl iodides by sequential C-H borylation and iodination is reported. The regioselectivity of this process is controlled by steric effects on the C-H borylation step and is complementary to existing methods to form aryl iodides. The iodination of boronic esters has potential for the synthesis of radiolabeled aryl iodides, as demonstrated by the concise synthesis of a potential tracer for SPECT imaging.

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