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Phenol, 2,6-diiodo-4-(1-methylethyl)-, also known as 2,6-diiodo-4-tert-butylphenol, is an organic compound with the chemical formula C10H12I2O. It is a white crystalline solid that is soluble in organic solvents and has a molecular weight of 393.02 g/mol. Phenol, 2,6-diiodo-4-(1-methylethyl)- is characterized by the presence of two iodine atoms at the 2nd and 6th positions of the phenol ring, and a tert-butyl group (1-methylethyl) attached to the 4th position. It is primarily used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and potential applications, it is important to handle Phenol, 2,6-diiodo-4-(1-methylethyl)- with care, as it may have toxic effects and should be stored away from heat and open flames.

2432-19-1

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2432-19-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2432-19-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2432-19:
(6*2)+(5*4)+(4*3)+(3*2)+(2*1)+(1*9)=61
61 % 10 = 1
So 2432-19-1 is a valid CAS Registry Number.

2432-19-1SDS

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 2.6-Diiod-4-isopropyl-phenol

1.2 Other means of identification

Product number -
Other names 2,6-Diiod-4-isopropylphenol

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:2432-19-1 SDS

2432-19-1Upstream product

2432-19-1Downstream Products

2432-19-1Relevant academic research and scientific papers

One-pot synthesis of 2,2′-bisbenzofurans using cuprous chloride as a catalyst

Pan, Wen-Bin,Chen, Chin-Chau,Wei, Li-Lan,Wei, Li-Mei,Wu, Ming-Jung

, p. 2655 - 2657 (2013)

A variety of novel 5,5′-disubstituted-2,2′-bisbenzofuran derivatives were synthesized by treatment of 4-substituted-2-(2- trimethylsilylethynyl)phenyl tert-butyldimethylsilyl ether analogues with CuCl as a catalyst in 62-82% isolated yields. This novel st

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