202821-16-7 Usage
Description
(2-tert-butylphenoxy)acetonitrile is a chemical compound with the molecular formula C12H15NO. It is a white solid at room temperature, insoluble in water, but soluble in organic solvents. (2-tert-butylphenoxy)acetonitrile is known for its use as a precursor in the synthesis of other organic compounds and for exhibiting a range of biological activities, making it a candidate for drug development and medicinal chemistry.
Uses
Used in Pharmaceutical Industry:
(2-tert-butylphenoxy)acetonitrile is used as a precursor in the synthesis of pharmaceutical compounds for its ability to contribute to the development of new drugs.
Used in Agrochemical Industry:
(2-tert-butylphenoxy)acetonitrile is used as a precursor in the synthesis of agrochemicals, playing a role in the creation of substances that can be used in agricultural applications.
Used in Research and Development:
(2-tert-butylphenoxy)acetonitrile is used as a research compound for studying its biological activities and potential applications in drug development and medicinal chemistry.
Safety Measures:
It is important to handle and use (2-tert-butylphenoxy)acetonitrile with appropriate safety measures in place, as it can pose health and environmental risks if not handled properly.
Check Digit Verification of cas no
The CAS Registry Mumber 202821-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,8,2 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 202821-16:
(8*2)+(7*0)+(6*2)+(5*8)+(4*2)+(3*1)+(2*1)+(1*6)=87
87 % 10 = 7
So 202821-16-7 is a valid CAS Registry Number.
202821-16-7Relevant articles and documents
Cytosine analogues from substituted acetonitriles via Thorpe condensation
Barkin, Julia L.,Faust Jr., Marcus D.,Trenkle, William C.
, p. 3333 - 3335 (2007/10/03)
(Matrix presented) A Thorpe condensation is the key bond construction in a rapid and efficient synthesis of substituted cytosine derivatives from readily available starting materials.