865374-17-0 Usage
Description
Bromo-3-tert-pentylbenzene is a chemical compound that features a benzene ring with a tert-pentyl group and a bromine atom attached at the 3-position. It is recognized for its high reactivity and stability, which makes it a valuable component in the synthesis of more complex molecules.
Uses
Used in Organic Synthesis:
Bromo-3-tert-pentylbenzene serves as a building block in organic synthesis, where it is utilized as a precursor for constructing more intricate molecular structures. Its reactivity and stability are key factors that facilitate the creation of a wide range of compounds.
Used in Pharmaceutical Industry Research and Development:
In the pharmaceutical sector, bromo-3-tert-pentylbenzene is employed for research and development purposes. It aids in the discovery and design of new pharmaceutical compounds, potentially leading to advancements in drug development.
Used in Specialty Chemicals Production:
Bromo-3-tert-pentylbenzene also finds application in the production of specialty chemicals. Its unique properties allow it to be a crucial component in the formulation of specific chemical products that cater to various industries.
It is crucial to handle bromo-3-tert-pentylbenzene with care, adhering to proper safety protocols and guidelines to ensure the safety of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 865374-17-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,3,7 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 865374-17:
(8*8)+(7*6)+(6*5)+(5*3)+(4*7)+(3*4)+(2*1)+(1*7)=200
200 % 10 = 0
So 865374-17-0 is a valid CAS Registry Number.
865374-17-0Relevant articles and documents
Access to "friedel-Crafts-Restricted" tert -alkyl aromatics by activation/methylation of tertiary benzylic alcohols
Hartsel, Joshua A.,Craft, Derek T.,Chen, Qiao-Hong,Ma, Ming,Carlier, Paul R.
, p. 3127 - 3133 (2012/05/20)
Herein we describe a two-step protocol to prepare m-tert-alkylbenzenes. The appropriate tertiary benzylic alcohols are activated with SOCl2 or concentrated HCl and then treated with trimethylaluminum, affording the desired products in 68-97% yields (22 examples). This reaction sequence is successful in the presence of a variety of functional groups, including acid-sensitive and Lewis-basic groups. In addition to t-Bu groups, 1,1-dimethylpropyl and 1-ethyl-1-methylpropyl groups can also be installed using this method.
