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2-Nitro(dichloroiodo)benzene is an organic compound with the chemical formula C6H3Cl2INO2. It is a derivative of benzene, featuring a nitro group (-NO2) at the 2nd carbon position, a dichloroiodo group (-Cl2I) at the 4th carbon position, and a hydroxyl group (-OH) at the 1st carbon position. 2-nitro(dichloroiodo)benzene is characterized by its yellowish color and has a molecular weight of 326.44 g/mol. It is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive nature, it is typically handled with care in controlled laboratory settings.

827-28-1

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827-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 827-28-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 827-28:
(5*8)+(4*2)+(3*7)+(2*2)+(1*8)=81
81 % 10 = 1
So 827-28-1 is a valid CAS Registry Number.

827-28-1Upstream product

827-28-1Relevant academic research and scientific papers

Development of Imino-λ3-iodanes with Improved Reactivity for Metal-Free [2+2+1] Cycloaddition-Type Reactions

Baba, Takafumi,Takahashi, Shunsuke,Kambara, Yui,Yoshimura, Akira,Nemykin, Victor N.,Zhdankin, Viktor V.,Saito, Akio

, p. 3860 - 3864 (2017)

Aiming at the enhancement of electrophilicity of imino-λ3-iodanes, we have developed (tosylimino)pentafluorophenyl-λ3-iodane, which shows superior reactivity compared to the commonly used (tosylimino)phenyl-λ3-iodane in the [2+2+1]-type synthesis of imidazoles. (Figure presented.).

Ceric ammonium nitrate as the novel oxidizing agent for the facile synthesis of (dichloroiodo)arenes

Tale, Nilesh P.,Shelke, Amol V.,Karade, Nandkishor N.

experimental part, p. 2959 - 2965 (2012/07/27)

Ceric ammonium nitrate (CAN) has been found to be a remarkable oxidizing agent for the oxidative conversion of iodoarenes to (dichloroiodo)arenes in acetic acid using aqueous HCl. The reaction of CAN with HCl generates in situ molecular chlorine, which is responsible for the oxidation. This method avoids the use of hazardous, toxic, and corrosive gaseous chlorine.

Novel oxidative, liquid-phase chlorination procedures for the preparation of (dichloroiodo)arenes from iodoarenes

Obeid,Skulski

, p. 1609 - 1615 (2007/10/03)

One improved and eight novel oxidative, liquid-phase chlorination procedures for the preparation of (dichloroiodo)arenes, ArICl2, from iodoarenes, ArI, are presented. KMnO4, activated MnO2, KCIO3, NaIO4/su

Liquid-phase and biphasic chlorination of some iodoarenes to form (dichloroiodo)arenes with sodium peroxodisulfate as the oxidant

Baranowski,Plachta,Skulski,Klimaszewska

, p. 435 - 437 (2007/10/03)

Liquid-phase and biphasic (CCl4/concd hydrochloric acid) chlorination of some iodoarenes to form the corresponding (dichloroiodo)arenes, prepared in 60-100% crude yields, are reported; dichlorine is produced as follows: Na2S2OP8 + 2 HCl (conc. aq.) → Cl2 + 2 NaHSO4.

Oxidative chlorination of various lodoarenes to (dichloroiodo)arenes with chromium(vi) oxide as the oxidant j

Kazmierczak, Pawet,Skulski, Lech,Obeid, Nicolas

, p. 64 - 65 (2007/10/03)

Chromium(vi) oxide dissolved in a mixture of acetic acid with concentrated hydrochloric acid converts, at or near room temperature, iodoarenes to (dichloroiodo)arenes, in a very simple and efficient procedure.

Biphasic chlorination of iodoarenes to (dichloroiodo)arenes

Krassowska-?wiebocka, Barbara,Prokopienko, Grazyna,Skulski, Lech

, p. 1409 - 1410 (2007/10/03)

A two-phase (CCl4/conc. hydrochloric acid) chlorination of some iodoarenes to the corresponding (dichloroiodo)arenes, prepared in 50-98% crude yields, is reported. Dichlorine is produced in the aqueous phase as follows: KClO3 (solid) + 6 HCl (conc. aq.) → ↑3Cl2 + KCl + 3H2O.

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