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3,4,5-3',4',5'-Hexachlordiazoaminobenzene, also known as HCBz, is a synthetic chemical compound characterized by its hexachlorinated structure and diazo group. It is a derivative of aminobenzene, with each of the three benzene rings bearing three chlorine atoms, and a diazo group (-N=N-) connecting the two rings. 3,4,5-3',4',5'-Hexachlordiazoaminobenzene is of interest in chemical research due to its unique structure and potential applications in various fields, such as materials science and pharmaceuticals. However, due to its complex and highly chlorinated nature, it may also raise concerns regarding environmental and health impacts, similar to other persistent organic pollutants. The compound's properties, such as solubility, stability, and reactivity, are influenced by its molecular structure, making it a subject of study for chemists to understand its behavior and potential uses.

898-27-1

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898-27-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 898-27-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,9 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 898-27:
(5*8)+(4*9)+(3*8)+(2*2)+(1*7)=111
111 % 10 = 1
So 898-27-1 is a valid CAS Registry Number.

898-27-1Upstream product

898-27-1Downstream Products

898-27-1Relevant academic research and scientific papers

Nitrosation with Sodium Hexanitrocobaltate(III)

Stefane, Bogdan,Kocevar, Marijan,Polanc, Slovenko

, p. 7165 - 7169 (1997)

Na3Co(NO2)6 has been investigated as a new reagent for the nitrosation of various substrates containing an amino functionality. Reactions took place in an aqueous solution of the reagent. The pH of the reaction mixture remained in the range 4.3-5. Thus, hydrazides were transformed to the corresponding acyl azides, and the reactions with arenesulfonyl hydrazines afforded arenesulfonyl azides. Treatment of aromatic amines with Na3Co(NO2)6 gave 1,3-diaryltriazenes in excellent yields; coupling of the initially formed diazo compound to the electron rich aromatic ring was also observed. Nitrosation of aliphatic amines was not possible due to complex formation with the reagent.

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