116314-71-7 Usage
Structure
Benzene ring with two hydroxyl groups (-OH) at positions 1 and 2, a hydroxymethyl group (-CH2OH) at position 5, and a nitro group (-NO2) at position 3.
Pharmaceuticals
Used in the production of certain pharmaceuticals.
Hair Dyes
Utilized in the formulation of hair dyes.
Photographic Development
Employed in the development of photographic materials.
Colorimetric Reagent
Serves as a colorimetric reagent for the detection of pyridine.
Industrial Uses
Wide range of uses in various industries, including pharmaceuticals, cosmetics, and photography.
Organic Synthesis
Acts as a building block for the creation of various organic compounds.
Research and Development
Used in the study and development of new chemical compounds and processes.
Potential Applications
The compound may have further applications in the field of organic synthesis and other areas of chemistry, as it is a versatile building block.
Safety Precautions
As with any chemical compound, proper handling, storage, and safety measures should be taken to minimize risks associated with exposure or accidental release.
Check Digit Verification of cas no
The CAS Registry Mumber 116314-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,3,1 and 4 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 116314-71:
(8*1)+(7*1)+(6*6)+(5*3)+(4*1)+(3*4)+(2*7)+(1*1)=97
97 % 10 = 7
So 116314-71-7 is a valid CAS Registry Number.
116314-71-7Relevant articles and documents
PHARMACOLOGICALLY ACTIVE COMPOUNDS, METHODS FOR THE PREPARATION THEREOF AND COMPOSITIONS CONTAINING THE SAME
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, (2008/06/13)
Pharmacologically active catechol derivatives of formula I I wherein R1 and R2 independently comprise hydrogen, alkyl, acyl, optionally substituted aroyl, lower alkylsulfonyl or alkylcabamoyl or taken together form a lower alkylidene or cycloalkylidene, X comprises an electronegative substituent such as halogen, nitro, cyano, lower alkylsulfonyl, sulfonamido, aldehyde, caboxyl or trifluoromethyl and R3 comprises hydrogen, halogen, hydroxy alkyl, amino, nitro, cyano, trifluoromethyl, lower alkylsulfonyl, sulfonamide, aldehyde, alkyl carbonyl, aralkylidene carbonyl or carboxyl or a group selected from wherein R4 comprises hydrogen, alkyl, cyano, carboxyl or acyl and R5 comprises hydrogen, cyano, carboxyl, alkoxycarbonyl, carboxyalkenyl, nitro, acyl, optionally substituted aroyl or heteroaroyl, hydroxyalkyl or carboxyalkyl or R4 and R5 together form a five to seven membered substituted cycloalkanone ring; -(CO)n(CH2)m-COR wherein n is 0-1 and m is 0-7 and R comprises hydroxy, alkyl, carboxyalkyl, optionally substituted alkene, alkoxy or optionally substituted amino; wherein R8 and R9 independently comprise hydrogen or one of the following optionally substituted groups; alkyl, alkenyl, alkynyl, cycloalkyl, aralkyl, or together form an optionally substituted piperidyl group; -NH-CO-R10 wherein R10 comprises a substituted alkyl group
