666459
6-Indolylboronic acid
≥95%
Synonym(s):
6-Indoleboronic acid, Indole-6-boronic acid
Sign Into View Organizational & Contract Pricing
All Photos(1)
Select a Size
Change View
1 G
$107.00
About This Item
Linear Formula:
(C8H6N)B(OH)2
CAS Number:
Molecular Weight:
160.97
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
![[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)](/deepweb/assets/sigmaaldrich/product/structures/130/734/8846aa26-1858-458a-998d-8c306c13bf0f/640/8846aa26-1858-458a-998d-8c306c13bf0f.png)
![[1,1′-Bis(di-tert-butylphosphino)ferrocene]dichloropalladium(II) 98%](/deepweb/assets/sigmaaldrich/product/structures/192/459/02d1239c-1119-49d9-b392-a04d8f53855c/640/02d1239c-1119-49d9-b392-a04d8f53855c.png)
Quality Level
assay
≥95%
form
powder
mp
177-181 °C
storage temp.
2-8°C
SMILES string
OB(O)c1ccc2cc[nH]c2c1
InChI
1S/C8H8BNO2/c11-9(12)7-2-1-6-3-4-10-8(6)5-7/h1-5,10-12H
InChI key
ZVMHOIWRCCZGPZ-UHFFFAOYSA-N
Related Categories
Application
Reactant involved in synthesis of:
Reactant involved in Suzuki-Miyaura reactions
- Indole compounds for use as HIV-1 glycoprotein-41 fusion inhibitors
- δ-Carbolines / carbozoles
- Trisubstituted pyrimidines as PI3K inhibitors
- (Thienopyridine)carboxamides as CHK1 inhibitors
- cis-Fluorostilbenes
Reactant involved in Suzuki-Miyaura reactions
Used in a study of racemization in Suzuki cross-couplings of arylamino acids.[1]
Other Notes
May contain varying amounts of anhydride
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Monica Prieto et al.
The Journal of organic chemistry, 72(3), 1047-1050 (2007-01-27)
Reaction conditions considered to be typical in Suzuki couplings can cause significant (up to 34% of the unwanted enantiomer) loss of optical purity in sensitive substrates such as hydroxyphenylglycine 1. This may be remedied using sodium succinate instead of sodium
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
