Welcome to LookChem.com Sign In|Join Free
  • or
1-iodo-3-Methoxy-2-Methylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21093-09-4

Post Buying Request

21093-09-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

21093-09-4 Usage

Classification

Organic compound.

Derivative

A derivative of toluene.

Constituents

Contains an iodine atom, a methoxy group, and a methyl group attached to a benzene ring.

Usage

Commonly used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds.

Application

Serves as a building block in organic synthesis.

Reactivity

Capable of undergoing various chemical reactions to form new compounds.

Hazardous Nature

Considered a hazardous chemical.

Precautions

Should be handled and stored with caution due to its toxic and irritant properties.

Check Digit Verification of cas no

The CAS Registry Mumber 21093-09-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,9 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21093-09:
(7*2)+(6*1)+(5*0)+(4*9)+(3*3)+(2*0)+(1*9)=74
74 % 10 = 4
So 21093-09-4 is a valid CAS Registry Number.

21093-09-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-iodo-3-methoxy-2-methylbenzene

1.2 Other means of identification

Product number -
Other names 2-iodo-6-methoxytoluene

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:21093-09-4 SDS

21093-09-4Downstream Products

21093-09-4Relevant academic research and scientific papers

Synthesis of complex ortho-allyliodoarenes by employing the reductive iodonio-claisen rearrangement

Khatri, Hem Raj,Zhu, Jianglong

supporting information, p. 12232 - 12236 (2012/11/07)

The reductive iodonio-Claisen rearrangement (RICR), involving complex aromatic λ3-iodanes and allyltrimethylsilane, was investigated. The RICR reaction of complex substituted aromatic hypervalent iodine (III) compounds and an allylmetal partner was conducted. The anionic oxy Cope rearrangement was found to be approximately 1010 to 1017 times faster than the neutral oxy Cope rearrangement due to weakening of the adjacent C-C bond by the oxygen anion. The results also indicate that the steric and electronic nature of the aromatic λ3-iodanes is the dominant factor influencing the [3,3]-sigmatropic rearrangement reaction. The removal of tert-butyl ether protecting group by using trifluroacetic acid in dichloromethane in the presence of triisopropylsilane gives the natural product broussin in 39% yield.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 21093-09-4