130511-67-0 Usage
Explanation
The compound consists of 6 carbon atoms, 3 hydrogen atoms, and 1 nitrogen atom, with 3 bromine atoms attached to the carbon atoms.
Explanation
It is a modified version of the five-membered aromatic heterocycle pyrrole.
Explanation
The compound contains a ring structure with alternating single and double bonds, which includes one or more heteroatoms (in this case, nitrogen) breaking the conjugation.
Explanation
A cyano group (C≡N) is attached to one of the carbon atoms, which can participate in various chemical reactions and contributes to the compound's properties.
Explanation
1H-Pyrrole-2-carbonitrile, 3,4,5-tribromois commonly used as an intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds.
Explanation
The compound is also utilized in the manufacturing of dyes, pigments, and other industrial chemicals due to its unique properties and reactivity.
Explanation
The presence of bromine atoms and the cyano group makes the compound highly reactive, which can be useful in various chemical reactions but also requires careful handling.
Explanation
Due to its brominated nature, the compound may exhibit toxic properties and should be handled with appropriate safety precautions.
Explanation
Proper handling and usage of 1H-Pyrrole-2-carbonitrile, 3,4,5-tribromoare essential to minimize potential health risks and environmental contamination.
Check Digit Verification of cas no
The CAS Registry Mumber 130511-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,5,1 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 130511-67:
(8*1)+(7*3)+(6*0)+(5*5)+(4*1)+(3*1)+(2*6)+(1*7)=80
80 % 10 = 0
So 130511-67-0 is a valid CAS Registry Number.
130511-67-0Relevant academic research and scientific papers
Wischang, Diana,Hartung, Jens
, p. 4048 - 4054 (2011)
Ester-, cyano-, and carboxamide-substituted 1H-pyrroles undergo electrophilic aromatic bromination, if treated with hydrogen peroxide and sodium bromide at pH 6.2 and 20 °C. Oxidation of bromide under such conditions is catalyzed by a vanadate(V)-dependent bromoperoxidase, in a substrate/enzyme ratio of 32-63 μmol %. To obtain maximum yields of bromopyrroles (up to 91%) by spending least amount of substrates and catalyst, hydrogen peroxide and sodium bromide have to be added continuously to the enzyme and the 2-acceptor-substituted pyrrole (1.5 mmol) in a solution of morpholine-4- ethanesulfonic acid buffer. This technique was applied to prepare two marine natural products under biomimetic conditions, that is, methyl 4,5-dibromopyrrole-2-carboxylate (from Agelas oroides) and 4,5-dibromopyrrole-2- carboxamide (from Acanthella carteri).
