19989-17-4 Usage
Uses
Used in Organic Synthesis:
2,2-DIMETHYL-6-NITROCHROMANE is used as a building block in organic synthesis for the creation of new compounds and materials. Its unique structure allows for further chemical reactions and modifications, contributing to the development of novel organic compounds with potential applications in various industries.
Used in Material Development:
In the field of material development, 2,2-DIMETHYL-6-NITROCHROMANE is utilized as a precursor for the synthesis of advanced materials. Its properties and reactivity can be harnessed to produce materials with specific characteristics, such as improved stability, reactivity, or selectivity.
Used in Pharmaceutical Industry:
2,2-DIMETHYL-6-NITROCHROMANE is used as a starting material or intermediate in the pharmaceutical industry for the synthesis of drug candidates. Its chemical structure may offer unique pharmacological properties, making it a valuable component in the development of new medications.
Used in Agrochemical Industry:
In the agrochemical industry, 2,2-DIMETHYL-6-NITROCHROMANE may be employed as a component in the synthesis of agrochemicals, such as pesticides or herbicides. Its potential reactivity and compatibility with other compounds can contribute to the development of effective and environmentally friendly agrochemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 19989-17-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,8 and 9 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19989-17:
(7*1)+(6*9)+(5*9)+(4*8)+(3*9)+(2*1)+(1*7)=174
174 % 10 = 4
So 19989-17-4 is a valid CAS Registry Number.
19989-17-4Relevant academic research and scientific papers
Synthesis and Antimicrobial Activity of Some 2-Amino-4-aryl-5-chromanylazothiazoles
Ahluwalia, V. K.,Singh, Raj P.,Singh, Rishi P.
, p. 287 - 289 (2007/10/02)
The title compounds have been synthesised by the condensation of diazotised 6-amino-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran with different 2-amino-4-arylthiazoles which in turn have been prepared by cyclocondensation of acetophenones with thiourea in the
