30158-45-3 Usage
Explanation
The molecular formula represents the number of atoms of each element present in the compound.
Explanation
The compound is derived from benzene, a basic structure in organic chemistry.
Explanation
The bromine atom is located at the first carbon position of the benzene ring.
Explanation
The sulfonyl group (-SO2-) is connected to the fourth carbon position of the benzene ring.
Explanation
The sulfonyl group has a 2-chloro-2-phenylethyl substituent, which adds complexity to the molecule.
Explanation
The compound is used as a building block for more complex molecules in organic synthesis.
Explanation
It is used in pharmaceutical research for the development of new drugs.
Explanation
The compound can be used as an intermediate in the production of various products, including pharmaceuticals, agrochemicals, and materials for scientific applications.
Explanation
Due to its complex structure and potential reactivity, it is essential to handle the compound carefully and follow safety guidelines to prevent accidents or harm.
Benzene derivative
Yes
Bromine atom
Attached to the 1 position
Sulfonyl group
Attached to the 4 position
Sulfonyl group substituent
2-chloro-2-phenylethyl
Use in organic synthesis
Yes
Pharmaceutical research
Yes
Potential applications
Pharmaceuticals, agrochemicals, and materials science
Safety precautions
Handle with care and follow proper safety protocols
Check Digit Verification of cas no
The CAS Registry Mumber 30158-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,5 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30158-45:
(7*3)+(6*0)+(5*1)+(4*5)+(3*8)+(2*4)+(1*5)=83
83 % 10 = 3
So 30158-45-3 is a valid CAS Registry Number.
30158-45-3Relevant academic research and scientific papers
Cu-Catalyzed photoredox chlorosulfonation of alkenes and alkynes
Alkan-Zambada, Murat,Hu, Xile
, p. 4525 - 4533 (2019/04/25)
Visible-light photoredox chlorosulfonation of alkenes and alkynes is achieved using a Cu photocatalyst. The reactions occur under mild conditions, have broad scope, and have high functional group tolerance.
