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2-Iodo-4-methylquinoline is an organic compound with the chemical formula C10H8IN. It is a derivative of quinoline, a heterocyclic aromatic compound with a benzene ring fused to a pyridine ring. The molecule features a methyl group at the 4-position and an iodine atom at the 2-position, which significantly influences its chemical properties and reactivity. 2-iodo-4-methylquinoline is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its unique structure, 2-iodo-4-methylquinoline has potential applications in the development of new drugs and materials, making it an important compound in the field of organic chemistry.

607-65-8

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607-65-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 607-65-8 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 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 607-65:
(5*6)+(4*0)+(3*7)+(2*6)+(1*5)=68
68 % 10 = 8
So 607-65-8 is a valid CAS Registry Number.

607-65-8SDS

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 2-iodo-4-methylquinoline

1.2 Other means of identification

Product number -
Other names 2-iodo-4-methyl-quinoline

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:607-65-8 SDS

607-65-8Relevant academic research and scientific papers

Microwave-assisted trans-halogenation reactions of various chloro-, bromo-, trifluoromethanesulfonyloxy- and nonafluorobutanesulfonyloxy-substituted quinolines, isoquinolines, and pyridines leading to the corresponding iodinated heterocycles

Bissember, Alex C.,Banwell, Martin G.

supporting information; experimental part, p. 4893 - 4895 (2009/10/02)

(Chemical Equation Presented) Microwave irradiation of certain chloro-, bromo-, trifluoromethanesulfonyloxy- and nonafluorobutanesulfonyloxy-substituted quinolines in the presence of acetic anhydride and sodium iodide leads, via a trans-halogenation process, to the corresponding iodides in high yield. Related conversions involving pyridines and isoquinolines can also be achieved under similar conditions.

Studies on Pyrimidine Derivatives. XXX. The Palladium-Catalyzed Cross-Coupling Reaction of Iodopyrimidines with Terminal Olefinic Compounds

Sakamoto, Takao,Arakida, Hiroko,Edo, Kiyoto,Yamanaka, Hiroshi

, p. 3647 - 3656 (2007/10/02)

The influence of triphenylphosphine, used as a ligand, on the palladium-catalyzed cross-coupling reaction of iodopyrimidines with olefins such as ethyl acrylate, acrylonitrile, and styrene was investigated.In general, the addition of triphenylphosphine was concluded to retard the reaction in the pyrimidine series.The effect of triphenylphosphine in the monoazine series is also discussed.Keywords - palladium catalyst; carbon-carbon bond formation; homo-coupling reaction of N-heteroaromatic iodide; raction conditions; six-membered N-heteroaromatic iodide; substituted ethenylpyrimidine

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