19752-21-7 Usage
Uses
Used in Pharmaceutical Industry:
2-METHOXY-2-METHYLPROPYL BROMIDE is used as a synthetic intermediate for the production of various pharmaceuticals. Its unique reactivity allows it to be a key component in the synthesis of a wide range of medicinal compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 2-METHOXY-2-METHYLPROPYL BROMIDE is utilized as an intermediate in the synthesis of different agrochemicals. Its role in creating effective pesticides and other agricultural chemicals is vital for enhancing crop protection and yield.
Used in Specialty Chemicals Production:
2-METHOXY-2-METHYLPROPYL BROMIDE is also employed in the manufacturing of specialty chemicals, which are used in a variety of applications across industries such as plastics, coatings, and fragrances. Its versatility in organic synthesis makes it an indispensable component in these chemical productions.
It is important to handle 2-METHOXY-2-METHYLPROPYL BROMIDE with care due to its potential hazards. It is classified as harmful if swallowed or inhaled and can cause skin and eye irritation upon contact, necessitating proper safety measures during its use and storage.
Check Digit Verification of cas no
The CAS Registry Mumber 19752-21-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,5 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19752-21:
(7*1)+(6*9)+(5*7)+(4*5)+(3*2)+(2*2)+(1*1)=127
127 % 10 = 7
So 19752-21-7 is a valid CAS Registry Number.
19752-21-7Relevant academic research and scientific papers
Method for synthesis and 99m C labelling of 2-alkoxyisobutylisonitrile
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, (2008/06/13)
A new method for synthesizing 2-alkoxyisobutylisonitrile is provided in which isobutylene is used as the starting material. The haloalkoxylation of isobutylene in alcohol medium gives 2-alkoxyisobutylhalide which is then converted to 2-alkoxyisobutylamine. In the basic condition, the reaction of 2-alkoxyisobutylamine with chloroform produces 2-alkoxyisobutylisonitrile. The synthesis process contains three steps by which a higher yield is achieved. 2-Alkoxyisobutylisonitrile is labelled with technetium-99m by exchange labelling of stable tetrakis(2-alkoxyisobutylisonitrile)copper(I) complex. Tetrakis(2-alkoxyisobutylisonitrile)copper(I) complex can be prepared by the exchange of acetonitrile molecules in tetrakis(acetonitrile)copper(I) complex with isonitrile ligands.
