945256-29-1 Usage
General Description
1H-Pyrrolo[2,3-b]pyridine, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- is a chemical compound commonly used in the field of organic chemistry for various applications. It is a heterocyclic compound containing a pyrrolopyridine ring system with a boron-containing substituent. 1H-Pyrrolo[2,3-b]pyridine, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- has shown potential as a building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. The boron-containing group in this compound is particularly useful for cross-coupling reactions and functional group transformations, making it a valuable tool for chemical synthesis. Additionally, this compound has been studied for its potential biological activities and has shown promise in certain medicinal chemistry applications. Overall, 1H-Pyrrolo[2,3-b]pyridine, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- is a versatile and valuable compound in organic chemistry with a wide range of potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 945256-29-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,2,5 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 945256-29:
(8*9)+(7*4)+(6*5)+(5*2)+(4*5)+(3*6)+(2*2)+(1*9)=191
191 % 10 = 1
So 945256-29-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H17BN2O2/c1-12(2)13(3,4)18-14(17-12)10-8-16-11-9(10)6-5-7-15-11/h5-8H,1-4H3,(H,15,16)
945256-29-1Relevant articles and documents
IMPROVED PROCESS FOR PREPARING BORYL 7-AZAINDOLE COMPOUNDS
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Page/Page column 22, (2016/12/22)
The present disclosure relates to an improved process for the preparation of 3-boryl substituted azaindole compounds in high yields and high selectivity. Such azaindole compounds may be used as intermediates to form compounds with cytotoxic, anticancer, and antiviral activities.
A traceless directing group for C - H borylation
Preshlock, Sean M.,Plattner, Donald L.,Maligres, Peter E.,Krska, Shane W.,Maleczka Jr., Robert E.,Smith III, Milton R.
supporting information, p. 12915 - 12919 (2014/01/06)
Not a trace: Borylation of the nitrogen in nitrogen heterocycles or anilines provides a traceless directing group for subsequent catalytic C - H borylation. Selectivities that previously required Boc protection can be achieved; furthermore, the NBpin directing group can be installed and removed in situ, and product yields are substantially higher. Boc=tert-butoxycarbonyl, pin=pinacolato. Copyright
