30771-71-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
Synonyms are alternative names for a chemical compound, often used to describe the same substance in different contexts or regions.
Explanation
The physical state describes the appearance and form of the compound, which in this case is a powder.
Explanation
The melting point is the temperature range at which the compound transitions from a solid to a liquid state.
Explanation
The compound is used as a building block in the synthesis of various pharmaceuticals and agrochemicals, indicating its importance in the development of these products.
Explanation
Pregabalin is a drug used to treat neuropathic pain and as an anti-epileptic medication, and its synthesis involves the use of 1,4-Benzenediol, 2-methyl-6-(phenylsulfonyl)-.
Explanation
The compound is utilized in the production of pesticides and herbicides, which are chemicals used to control pests and weeds in agriculture.
Explanation
The compound has applications in the production of dyes, pigments, and other specialty chemicals, which are used in various industries for coloring and other specific purposes.
Synonyms
Methyl-p-benzenediol-2-sulfonate
Physical State
White to off-white powder
Melting Point
168-172°C
Applications
Pharmaceutical and agrochemical synthesis
Specific Drug Synthesis
Pregabalin
Pesticides and Herbicides
Manufacturing
Dyes, Pigments, and Specialty Chemicals
Production
Check Digit Verification of cas no
The CAS Registry Mumber 30771-71-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,7 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30771-71:
(7*3)+(6*0)+(5*7)+(4*7)+(3*1)+(2*7)+(1*1)=102
102 % 10 = 2
So 30771-71-2 is a valid CAS Registry Number.
30771-71-2Relevant academic research and scientific papers
Ionic liquids-promoted addition of arylsulfinic acids to p-quinones: A green synthesis of diaryl sulfones
Yadav,Reddy,Swamy,Ramireddy
, p. 1849 - 1853 (2007/10/03)
Arylsulfinic acids undergo smooth conjugate addition to p-quinones in air- and moisture-stable second generation room temperature ionic liquid [bmim]BF4 under mild conditions to produce the corresponding arylsulfonylhydroquinones in excellent yields with high selectivity. In this reaction, ionic liquid plays the dual role as the solvent and the catalyst. The quinones show enhanced reactivity in ionic liquid thereby reducing the reaction times and improving the yields significantly. The presence of ionic liquids helps to avoid the use of either acid or base catalysts for this conversion. The recovered ionic liquid was reused for four to five times with consistent activity.
Regiospecificity in the synthesis of diaryl sulfones
Allgeier, Daniel E.,Herbert, Sue Ann,Nee, Rory,Schlecht, Kenneth D.,Finley, K. Thomas
, p. 4988 - 4990 (2007/10/03)
The addition of arylsulfinic acids to 2-methyl-1,4-benzoquinone provides high yields of sulfones in a wide variety of solvents. The distribution of isomeric products obtained is strongly influenced by either (1) the acidity of aqueous solvents or (2) the water content of alcohol solvents. The distribution of isomeric products does not change in the various anhydrous, aprotic solvents examined.
