52287-49-7 Usage
Functional Groups
Trimethylsilyl, Methoxy
Explanation
The compound contains a trimethylsilyl group (Si-(CH3)3) and two methoxy groups (O-CH3) attached to the benzene ring.
Explanation
The core structure of the compound is a benzene ring, which is a six-membered carbon ring with alternating single and double bonds.
Explanation
The benzene ring is substituted with a trimethylsilyl group at the 1st position and two methoxy groups at the 3rd and 4th positions.
Explanation
The compound is known for its ability to react with different functional groups, making it a versatile reagent in chemical reactions.
Explanation
It serves as a building block in the synthesis of a wide range of organic compounds.
Explanation
The presence of the trimethylsilyl group (Si-(CH3)3) on the benzene ring contributes to the stability and protection of the molecule.
Explanation
The trimethylsilyl group can act as a protecting agent for the molecule, shielding reactive sites during chemical reactions.
Explanation
Due to its non-polar nature, the compound is likely to be soluble in organic solvents such as dichloromethane, ethyl acetate, or toluene.
Aromatic Ring
Benzene
Substitution
1-(trimethylsilyl)-3,4-dimethoxy
Versatility
Reacts with various functional groups
Building Block
Used in organic synthesis
Applications
Pharmaceutical and materials science research
Stability
Provided by the trimethylsilyl group
Protection
Trimethylsilyl group as a protecting agent
Solubility
Likely soluble in organic solvents
Check Digit Verification of cas no
The CAS Registry Mumber 52287-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,8 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 52287-49:
(7*5)+(6*2)+(5*2)+(4*8)+(3*7)+(2*4)+(1*9)=127
127 % 10 = 7
So 52287-49-7 is a valid CAS Registry Number.
52287-49-7Relevant articles and documents
A convenient iron-catalyzed method for the preparation of 1,2-bis(trimethylsilyl)benzenes
Bader, Samuel L.,Kessler, Simon N.,Wegner, Hermann A.
experimental part, p. 2759 - 2762 (2010/10/05)
A convenient iron-catalyzed method for the preparation of 1,2-bis(trimethylsilyl)benzenes is presented. Compared to the current procedures, low temperatures and toxic solvents are avoided, allowing large-scale preparation. Additionally, a variety of subst
