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Isoquinoline, 7-iodo(9CI) is a chemical compound characterized by the molecular formula C9H6IN. It represents an iodinated derivative of the heterocyclic organic compound isoquinoline, which shares structural similarities with quinoline. Isoquinoline, 7-iodo(9CI) is distinguished by its unique reactivity and structural attributes, making it a valuable component in various chemical processes.

75476-83-4

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75476-83-4 Usage

Uses

Used in Organic Synthesis:
Isoquinoline, 7-iodo(9CI) is utilized as a key building block in organic synthesis, particularly for the creation of pharmaceuticals, agrochemicals, and other organic compounds. Its distinctive structure and reactivity contribute to the synthesis of a wide range of complex organic molecules.
Used in Chemical Reactions:
Isoquinoline, 7-iodo(9CI) is also employed in various chemical reactions due to its specific properties. Its iodine substituent enhances its reactivity, making it a versatile agent in the field of organic chemistry.
Used in Pharmaceutical Industry:
Isoquinoline, 7-iodo(9CI) is used as a chemical intermediate in the pharmaceutical industry for the development of new drugs. Its unique structure allows for the creation of novel therapeutic agents with potential applications in medicine.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, Isoquinoline, 7-iodo(9CI) serves as a precursor for the synthesis of new agrochemicals, contributing to the development of innovative products for agricultural applications.
Used in Research and Development:
Furthermore, Isoquinoline, 7-iodo(9CI) is a useful tool in research and development, particularly for studying organic reactions and mechanisms. Its iodine atom provides a means to probe and understand reaction pathways and intermediates, thus advancing the understanding of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 75476-83-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,7 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75476-83:
(7*7)+(6*5)+(5*4)+(4*7)+(3*6)+(2*8)+(1*3)=164
164 % 10 = 4
So 75476-83-4 is a valid CAS Registry Number.

75476-83-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-iodoisoquinoline

1.2 Other means of identification

Product number -
Other names 7-IODO-ISOQUINOLINE

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:75476-83-4 SDS

75476-83-4Downstream Products

75476-83-4Relevant academic research and scientific papers

NOVEL COMPOUNDS AS PHARMACEUTICAL AGENTS

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Page 37-38, (2010/02/07)

The current invention relates to compounds of the formula:(Ia) and the pharmaceutically acceptable salts thereof and their use as TGF-beta signal transduction inhibitors for treating cancer and other diseases in a patient in need thereof by administration of said compounds.

Synthesis of Isoquinolines from Indenes

Miller, R. Bryan,Frincke, James M.

, p. 5312 - 5315 (2007/10/02)

A general procedure for the synthesis of isoquinolines from appropriately substituted indenes is described.Ozonolysis of the indenes followed by reductive workup gives intermediate homophthalaldehydes which are treated with ammonium hydroxide to give the isoquinolines.This "one-pot", three-step reaction sequence was applied to the formation of all of the mono-C-methyl-substituted isoquinolines in a regiospecific manner.The procedure is applicable to both electron-withdrawing and electron-donating substituents on the indene system.In this manner the 6- and 7-nitro-,-bromo-, and -iodoisoquinolines were prepared.

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