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19099-56-0

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19099-56-0 Usage

General Description

3-Iodoisopropylbenzene is a chemical compound with the molecular formula C9H11I. It is a colorless liquid that is used primarily as a reagent in organic synthesis. 3-Iodoisopropylbenzene is an alkyl iodide, which means it has an iodine atom attached to a secondary carbon atom. As a result, it is often used in organic reactions that involve nucleophilic substitution and other synthetic pathways. 3-Iodoisopropylbenzene is also used in the production of pharmaceuticals, agrochemicals, and other fine chemicals due to its ability to serve as a building block in the synthesis of complex organic molecules. However, it is important to handle this compound with care, as it is considered to be a hazardous substance and can pose risks to human health and the environment if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 19099-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,9 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 19099-56:
(7*1)+(6*9)+(5*0)+(4*9)+(3*9)+(2*5)+(1*6)=140
140 % 10 = 0
So 19099-56-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H11I/c1-7(2)8-4-3-5-9(10)6-8/h3-7H,1-2H3

19099-56-0SDS

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 1-iodo-3-propan-2-ylbenzene

1.2 Other means of identification

Product number -
Other names 1-iodo-3-isopropylbenzene

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:19099-56-0 SDS

19099-56-0Upstream product

19099-56-0Relevant articles and documents

Synthesis of Azepino[1,2-a]indole-10-amines via [6+1] Annulation of Ynenitriles with Reformatsky Reagent

Iioka, Ryoya,Yorozu, Kohei,Sakai, Yoko,Kawai, Rika,Hatae, Noriyuki,Takashima, Katsuki,Tanabe, Genzoh,Wasada, Hiroaki,Yoshimatsu, Mitsuhiro

supporting information, p. 1553 - 1558 (2021/02/26)

Lewis acid-catalyzed [6+1] annulation reactions of 2-cyano-1-propargyl- and 2-alkynyl-1-cyanomethyl-indoles with Reformatsky reagent are described. 8-Aryl, 8-alkyl-, 8-hetaryl-, 9-aryl, and 9-alkyl-azepino[1,2-a]indole amines were obtained through a 7-endo-mode cyclization of the β-aminoacrylate intermediates. The antiproliferative activity of the azepino[1,2-a]indoles analogs against the HCT-116 cells were also examined.

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