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α,α-Dichlor-2-nitro-5-iodtoluol is an organic compound with the chemical formula C7H5Cl2INO2. It is a derivative of toluene, featuring two chlorine atoms attached to the alpha carbon (the carbon adjacent to the methyl group), a nitro group at the 2nd position, and an iodine atom at the 5th position. α,α-Dichlor-2-nitro-5-iodtoluol is characterized by its yellow crystalline appearance and has potential applications in chemical research and synthesis. Due to its reactive nature and the presence of multiple halogens, it may be used in the preparation of various intermediates or as a reagent in organic reactions. However, it is important to handle α,α-Dichlor-2-nitro-5-iodtoluol with care due to its potential toxicity and reactivity.

30669-52-4

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30669-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30669-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,6 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 30669-52:
(7*3)+(6*0)+(5*6)+(4*6)+(3*9)+(2*5)+(1*2)=114
114 % 10 = 4
So 30669-52-4 is a valid CAS Registry Number.

30669-52-4Downstream Products

30669-52-4Relevant academic research and scientific papers

Dihalomethylation of Nitroarenes via Vicarious Nucleophilic Substitution of Hydrogen with Trihalomethyl Carbanions

Makosza, M.,Owczarczyk, Z.

, p. 5094 - 5100 (2007/10/02)

Trichloro- and tribromomethyl carbanions generated by deprotonation of haloforms with potassium tert-butoxide in a THF-DMF mixture at ca. -70 deg C react with a variety of carbocyclic and heterocyclic nitroarenes according to the vicarious nucleophilic substitution scheme.The reaction provides an efficient and convenient way for the direct introduction of dihalomethyl substituents ortho and para to the nitro group, which in turn can be hydrolyzed to produce nitroaryl aldehydes.

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