608-29-7 Usage
Structure
A benzene ring with three iodine atoms attached in positions 1, 2, and 3
Organic chemistry
Used as a reagent for various chemical reactions
Synthesis
Used in the synthesis of other organic compounds
Pharmaceutical production
Used in the production of pharmaceuticals
Dye production
Used in the production of dyes
Industrial chemicals
Used in the production of other industrial chemicals
Hazard
Toxic and hazardous substance
Careful handling
Should be handled with care
Proper safety measures
Proper safety measures should be followed
Safety guidelines
Important to follow safety guidelines and regulations when working with this compound
Avoid exposure
To avoid exposure and potential harm
Physical state
Solid at room temperature (based on the general properties of halogenated benzenes)
Check Digit Verification of cas no
The CAS Registry Mumber 608-29-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 608-29:
(5*6)+(4*0)+(3*8)+(2*2)+(1*9)=67
67 % 10 = 7
So 608-29-7 is a valid CAS Registry Number.
608-29-7Relevant articles and documents
A simple and efficient two-step synthesis of 1,2,3-triiodoarenes via consecutive C-H iodination/ipso-Iododecarboxylation strategy: A potential application towards Ortho-diiodoarenes by Regioselective metal-iodine exchange reaction
Al-Zoubi, Raed M.,Al-Mughaid, Hussein,McDonald, Robert
, p. 912 - 918 (2015/06/25)
A general, robust, and efficient method for the conversion of benzoic acids to 1,2,3-triiodoarenes and 1,2,3-trihaloarenes via a two-step synthesis is reported. Commercially available benzoic acids were used that can allow the reactions to be performed on multi-gram scales with good-to-excellent yields. This report discloses a practical method for the synthesis of 1,2,3-triiodoarenes and 1,2,3-trihaloarenes that is general in scope, scalable, and easy to workup and purify. A potential application of the target compounds as precursors for novel regioselective metal-iodine exchange reaction of 1,2,3-triiodoarenes was also demonstrated. It provided ortho-diiodoaryl derivatives in a high regioselective fashion that are useful intermediates in synthesis and indeed are hard to synthesize by any other means.