1000068-66-5 Usage
Chemical class
Boronic acids
Explanation
Different sources of media describe the Explanation of 1000068-66-5 differently. You can refer to the following data:
1. This compound belongs to the class of boronic acids, which are known for their ability to form stable complexes with organic molecules.
2. It is commonly used in organic synthesis and medicinal chemistry due to its unique reactivity and binding properties.
3. The boronic acid functionality allows the compound to selectively bind with specific biological targets, making it potentially useful in the treatment of various diseases and conditions.
4. The presence of an ester group in the compound makes it a versatile building block for the synthesis of complex organic molecules.
5. The tert-butyl substituent contributes to the stability and reactivity of the compound, enhancing its potential as a building block in organic synthesis.
6. Due to its unique properties and reactivity, 1H-Indole-1-carboxylic acid, 2-borono-7-methyl-, 1-(1,1-dimethylethyl) ester is of interest for the development of new drugs and pharmaceuticals.
Application
Organic synthesis and medicinal chemistry
Boronic acid functionality
Selective binding with biological targets
Ester group
Versatile building block
Tert-butyl substituent
Stability and reactivity
Potential applications
Drug development and pharmaceuticals
Check Digit Verification of cas no
The CAS Registry Mumber 1000068-66-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,0,6 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1000068-66:
(9*1)+(8*0)+(7*0)+(6*0)+(5*0)+(4*6)+(3*8)+(2*6)+(1*6)=75
75 % 10 = 5
So 1000068-66-5 is a valid CAS Registry Number.
