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Benzene, 1-iodo-4-(2-methylpropyl)-, also known as iodoisobutylbenzene, is a chemical compound with the molecular formula C10H13I. It is a substituted aromatic compound characterized by a benzene ring to which a 1-iodo-4-(2-methylpropyl) group is attached. Benzene, 1-iodo-4-(2-methylpropyl)is recognized for its role as an intermediate in the synthesis of a variety of pharmaceuticals, agrochemicals, and other organic compounds. It also serves as a reagent in organic reactions and is a common component in research and industrial laboratories. Due to its potential toxicity and harmful effects, careful handling is essential when working with Benzene, 1-iodo-4-(2-methylpropyl)-.

85609-09-2

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85609-09-2 Usage

Uses

Used in Pharmaceutical Synthesis:
Benzene, 1-iodo-4-(2-methylpropyl)is utilized as an intermediate in the production of various pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of drugs that target specific medical conditions, contributing to the development of new and effective treatments.
Used in Agrochemical Production:
Benzene, 1-iodo-4-(2-methylpropyl)also plays a role in the creation of agrochemicals, which are chemicals used in agricultural processes such as pest control and crop enhancement. Its application in this industry helps to improve agricultural yields and protect crops from harmful organisms.
Used in Organic Reactions as a Reagent:
Benzene, 1-iodo-4-(2-methylpropyl)functions as a reagent in a range of organic reactions, facilitating the synthesis of complex organic molecules. Its presence can drive reactions forward, enabling the formation of desired products in research and industrial settings.
Used in Research and Industrial Laboratories:
As a common component in laboratories focused on chemical research and development, Benzene, 1-iodo-4-(2-methylpropyl)is vital for conducting experiments and developing new chemical processes. Its versatility in reactions makes it a valuable asset in the pursuit of scientific discovery and innovation.
Safety Considerations:
Given the potential toxicity and harmful nature of Benzene, 1-iodo-4-(2-methylpropyl)-, it is crucial to handle Benzene, 1-iodo-4-(2-methylpropyl)- with care. Proper safety measures, including the use of personal protective equipment and adherence to laboratory safety protocols, are essential to minimize risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 85609-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,0 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85609-09:
(7*8)+(6*5)+(5*6)+(4*0)+(3*9)+(2*0)+(1*9)=152
152 % 10 = 2
So 85609-09-2 is a valid CAS Registry Number.

85609-09-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-iodo-4-(2-methylpropyl)benzene

1.2 Other means of identification

Product number -
Other names Benzene,1-iodo-4-(2-methylpropyl)

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:85609-09-2 SDS

85609-09-2Relevant academic research and scientific papers

Tricyclic pyridine derivatives, medicaments containing such compounds, their use and process for their preparation

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Paragraph 2297-2300, (2013/03/26)

The present invention relates to compounds defined by formula I wherein the variables R1-R8 are defined as in the description, possessing valuable pharmacological activity. Particularly, the compounds are inhibitors of cholesterol ester transfer protein (CETP) and thus are suitable for treatment and prevention of diseases which can be influenced by inhibition of this enzyme.

TRICYCLIC PYRIDINE DERIVATIVES, MEDICAMENTS CONTAINING SUCH COMPOUNDS, THEIR USE AND PROCESS FOR THEIR PREPARATION

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Page/Page column 154, (2012/03/10)

The present invention relates to compounds defined by formula I wherein the variables R1-R8 are defined as in the description, possessing valuable pharmacological activity. Particularly, the compounds are inhibitors of cholesterol ester transfer protein (CETP) and thus are suitable for treatment and prevention of diseases which can be influenced by inhibition of this enzyme.

4-AMINO-5-OXO-7, 8-DIHYDROPYRIMIDO [5,4-F] [1,4] OXAZEPIN-6 (5H) -YL) PHENYL DERIVATIVES, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF

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Page/Page column 47-48, (2010/08/09)

The invention provides compounds of Formula (I), wherein R1, R2a, R2b, R3, m and A are as defined herein, as well as compositions thereof and methods for treating a disease, condition or disorder that is modulated by the inhibition of the diacylglycerol O-acyltransferase 1 (DGAT-1) enzyme by administering the compounds of the present invention and/or compositions thereof.

4-AMINO-7,8-DIHYDROPYRIDO[4,3-d]PYRIMIDIN-5(6H)-ONE DERIVATIVES

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Page/Page column 22, (2010/08/08)

The invention provides compounds of the general Formula (I) where R1, R2, and A are defined herein, as well as the preparation, compositions and uses thereof.

Lipase-mediated asymmetric construction of 2-arylpropionic acids: Enantiocontrolled syntheses of S-naproxen and S-ibuprofen

Bando, Toshikazu,Namba, Yukiko,Shishido, Kozo

, p. 2159 - 2165 (2007/10/03)

A general and enantiocontrolled synthetic route to 2-arylpropionic acids, represented by non-steroidal anti-inflammatory drugs S-naproxen 1a and S-ibuprofen 1b, has been developed by employing the lipase-mediated asymmetric acetylation of prochiral 2-aryl-1,3-propanediol 3, which has been derived via a Heck reaction, as the key step.

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