22807-80-3 Usage
General Description
1-Bromo-4-(tert-butoxymethyl)benzene is a chemical compound that consists of a benzene ring with a bromine atom and a tert-butoxymethyl group attached to it. It is commonly used as a reagent in organic synthesis and is known for its ability to undergo various reactions such as nucleophilic substitution and elimination. 1-Bromo-4-(tert-butoxymethyl)benzene is important in the pharmaceutical industry as it is a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also used in the production of polymers and dyes. Additionally, 1-Bromo-4-(tert-butoxymethyl)benzene has potential applications in materials science and as a building block for the synthesis of more complex organic compounds. However, it is important to handle this chemical with care as it is toxic and can cause irritation to the skin, eyes, and respiratory system.
Check Digit Verification of cas no
The CAS Registry Mumber 22807-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,0 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22807-80:
(7*2)+(6*2)+(5*8)+(4*0)+(3*7)+(2*8)+(1*0)=103
103 % 10 = 3
So 22807-80-3 is a valid CAS Registry Number.
22807-80-3Relevant articles and documents
Acid- and isobutylene-free synthesis of t-butyl ethers by in situ formation of 2-t-butoxy-1-methylpyridinium triflate
Salvati, Anna E.,Hubley, Christian T.,Albiniak, Philip A.
, p. 7133 - 7135 (2014)
The title reagent is formed in situ by alkylation of 2-t-butoxypyrine. The subsequent addition of an alcohol substrate leads to the formation of t-butyl ethers without the need for isobutylene gas or acid activators.
Propylene Random Copolymer
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Paragraph 0083-0085, (2020/12/04)
Provided is a propylene random copolymer having excellent processability. The propylene random copolymer according to the present invention may exhibit high stiffness and flexural modulus together with a low shrinkage ratio, thereby being usefully applied
Synthesis of Cyclo-bis; A Cholaphane with Reduced Flexibility and Externally-directed Functionality
Davis, Anthony P.,Orchard, Michael G.
, p. 919 - 924 (2007/10/02)
A second 'cholaphane' framework is manifested in the title compound 8, which has been prepared from methyl 3α,7α,12α-triacetoxycholanoate 9 in 23percent overall yield.The synthesis involves the Knoevenagel condensation of ketone 11 with malononitrile to g
