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1,4-Dibromo-2,6-dinitrobenzene is an organic compound characterized by the presence of two bromine atoms at the 1st and 4th carbon positions, and two nitro groups at the 2nd and 6th carbon positions on a benzene ring. This chemical is known for its high reactivity and is often used in the synthesis of various pharmaceuticals, dyes, and other organic compounds. Due to its hazardous nature, it is crucial to handle 1,4-Dibromo-2,6-dinitrobenzene with extreme care, as it can pose significant health risks and environmental concerns.

6310-99-2

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6310-99-2 Usage

Appearance

Yellow crystalline solid

Solubility

Insoluble in water and organic solvents

Uses

a. Reagent in organic synthesis
b. Production of dyes and pharmaceuticals

Chemical properties

a. Potent electrophile
b. Used in preparation of nitroaryl and nitro-substituted heterocyclic compounds

Toxicity

Toxic and a skin irritant

Health hazards

Causes irritation to skin, eyes, and respiratory system

Environmental impact

Potentially harmful to aquatic organisms and the environment

Safety precautions

Necessary when handling due to toxicity and irritant properties

Check Digit Verification of cas no

The CAS Registry Mumber 6310-99-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6310-99:
(6*6)+(5*3)+(4*1)+(3*0)+(2*9)+(1*9)=82
82 % 10 = 2
So 6310-99-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H2Br2N2O4/c7-3-1-4(9(11)12)6(8)5(2-3)10(13)14/h1-2H

6310-99-2Relevant articles and documents

Thermal Stability Studies on a Homologous Series of Nitroarenes

Oxley, Jimmie C.,Smith, James L.,Ye, Hong,McKenney, Robert L.,Bolduc, Paul R.

, p. 9593 - 9602 (2007/10/02)

The thermal stabilities of a number of nitroarenes were examined in solution and in condensed phase.In general, increasing the number of nitro groups decreased thermal stability.Changing the substituent on 1-X-2,4,6-trinitrobenzene from X = H to NH2 to CH3 to OH accelerated decomposition; this effect was attributed to increased ease of intramolecular proton transfer to an ortho nitro group, thus weakening the carbon-nitrogen bond.In solution, the effect of increasing substitution from n = 1 to n = 3 on Xn(NO2)3C6H3-n was uniformly that of decreasing the thermal stability of the species.However, in condensed phase, results suggested that crystal habit may be more important than molecular structure; for X = Br, CH3, and NH2, the more substituted species was the more stable.

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