1-Pyrenyl­boron­ic acid CAS 164461-18-1

• Iden­ti­fi­ca­tion
• Prop­er­ties
• Safe­ty Data
• Spec­i­fi­ca­tions & Oth­er Information
• Links
• Quick Inquiry

Iden­ti­fi­ca­tion

CAS Number

164461-18-1

Name

1-Pyrenyl­boron­ic acid

Syn­onyms

164461-18-1 [RN]
1-Pyreneboron­ic acid
1-Pyrenyl­boron­ic acid [ACD/IUPAC Name]
1-Pyrenyl­borsäure [Ger­man] [ACD/IUPAC Name]
Acide 1-pyrényl­boronique [French] [ACD/IUPAC Name]
Boron­ic acid, B-1-pyrenyl- [ACD/​Index Name]
L666 B6 2AB PJ GBQQ [WLN]
MFCD04974062 [MDL num­ber]
pyren-1-ylboron­ic acid
Pyrene-1-boron­ic acid
(pyren-1-yl)boronic acid
[164461-18-1] [RN]
1-Boronopy­­rene
1-Pyrene boron­ic acid
1-Pyreneboron­ic Acid (con­tains vary­ing amounts of Anhy­dride)
1-Pyreneboron­ic Acid (en)
1-Pyreneboron­i­­cAcid
1-Pyrenyl boron­ic acid
1-Pyrenyl­boron­i­­cacid
AGN-PC-0LM­C­QZ
BB-8011
Boron­ic acid, 1-pyrenyl-
GS-6482
POP­ULIN
PubChem16490
PYREN-1-YLBORON­IC ACID|(PYREN-1-YL)BORON­IC ACID
Pyrene-1-boron­ic acid|1-Boronopyrene
pyreneboron­ic acid
TL8001259

SMILES

B(c1ccc2ccc3cccc4c3c2c1cc4)(O)O

Std­InChI

InChI=1S/C16H11BO2/c18-17(19)14-9-7-12-5-4-10-2-1-3-11-6-8-13(14)16(12)15(10)11/h1-9,18-19H

Std­InChIKey

MWEK­­PLLM­FX­I­­ZOC-UHF­F­­FAOYSA-N

Mol­e­c­u­lar Formula

C₁₆H₁₁BO₂

Mol­e­c­u­lar Weight

246.068

MDL Number

MFCD04974062

Prop­er­ties

Appear­ance

Yel­low powder

Struc­ture

struc­ture of 1-Pyrenyl­boron­ic acid CAS 164461-18-1

Safe­ty Data

Sig­nal Word

Warn­ing

WGK Germany

3

MSDS Download

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our 

Iden­ti­fi­ca­tion Methods

HNMR, HPLC

Puri­ty

99.5% min

Lod

1%

Shelf Life

1 year

Stor­age

Cool, dry place with tight­en contairier

Known Appli­ca­tion

1-Pyrenyl­boron­ic acid can form coor­di­na­tion com­plex­es with met­al ions through the boron­ic acid group’s coor­di­na­tion abil­i­ty. These com­plex­es have impor­tant appli­ca­tions in catal­y­sis, mate­ri­als sci­ence, and bio­analy­sis.
1-Pyreneboron­ic acid can under­go car­bon-car­bon bond for­ma­tion reac­tions with suit­able reac­tants, such as organ­ic halides or aro­mat­ic alde­hy­des. This reac­tion is often employed in organ­ic syn­the­sis for car­bon-car­bon bond con­nec­tions and the con­struc­tion of com­plex organ­ic mol­e­cules. And due to the unique prop­er­ties of the pyrene mol­e­cule, 1-Pyreneboron­ic acid is com­mon­ly used as a flu­o­res­cence probe or emit­ting group in pho­to­phys­i­cal and pho­to­chem­i­cal stud­ies. Its flu­o­res­cence prop­er­ties make it wide­ly applic­a­ble in ana­lyt­i­cal chem­istry, biol­o­gy, and mate­ri­als science.

Gen­er­al View of Documents

Links

This prod­uct is devel­oped by our R&D com­pa­ny Warshel Chem­i­cal Ltd (https://​www​.warshel​.com/).

Quick Inquiry

Fill out our inquiry form and one of our experts will be in touch with you shortly.