30169-75-6 Usage
Type of compound
Boron-containing heterocyclic compound
Structure
Six-membered cyclohexyl ring fused to a five-membered dioxaborinane ring
Usage
Precursor for synthetic organic chemistry
Importance
Intermediate in the synthesis of various pharmaceuticals and agrochemicals
Application
Ligand for transition metal catalysts in organic synthesis
Development
Used in the development of new methodologies for carbon-carbon and carbon-heteroatom bond formation
Biological activity
Exhibits biological activity, potentially useful in medicinal chemistry and drug discovery
Check Digit Verification of cas no
The CAS Registry Mumber 30169-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,6 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30169-75:
(7*3)+(6*0)+(5*1)+(4*6)+(3*9)+(2*7)+(1*5)=96
96 % 10 = 6
So 30169-75-6 is a valid CAS Registry Number.
30169-75-6Relevant articles and documents
How Big is the Pinacol Boronic Ester as a Substituent?
Fasano, Valerio,McFord, Aidan W.,Butts, Craig P.,Collins, Beatrice S. L.,Fey, Natalie,Alder, Roger W.,Aggarwal, Varinder K.
supporting information, p. 22403 - 22407 (2020/10/12)
The synthetically versatile pinacol boronic ester group (Bpin) is generally thought of as a bulky moiety because of the two adjacent quaternary sp3-hydribized carbon atoms in its diol backbone. However, recent diastereoselective reactions repor
