Indole-6-boronic acid

Suppliers

Names

[ CAS No. ]:
147621-18-9

[ Name ]:
Indole-6-boronic acid

[Synonym ]:
Boronic acid, B-1H-indol-6-yl-
6-Indoleboronic Acid
MFCD03095176
6-Indolylboronic Acid
1H-Indol-6-ylboronic acid

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
433.2±37.0 °C at 760 mmHg

[ Melting Point ]:
177-181ºC

[ Molecular Formula ]:
C8H8BNO2

[ Molecular Weight ]:
160.966

[ Flash Point ]:
215.8±26.5 °C

[ Exact Mass ]:
161.064804

[ PSA ]:
56.25000

[ LogP ]:
1.51

[ Vapour Pressure ]:
0.0±1.1 mmHg at 25°C

[ Index of Refraction ]:
1.662

[ Storage condition ]:
Keep Cold

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933990090

Synthetic Route

Precursor & DownStream

Precursor

  • 6-bromoindole
  • BUTYL BORATE
  • Tert-Butyllithium
  • 6-Chloro-1H-indole

DownStream

  • 6-(PYRIDIN-3-YL)-1H-INDOLE

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Racemization in suzuki couplings: a quantitative study using 4-hydroxyphenylglycine and tyrosine derivatives as probe molecules.

J. Org. Chem. 72 , 1047, (2007)

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 hydroxyphenylglycin...


More Articles


Related Compounds

  • 1-TBDMS-indole-6-boronic acid
  • Indole-6-boronic acid pinacol ester
  • 4-Azaindole-6-boronic acid pinacol ester
  • CHROMONE-6-BORONIC ACID PINACOL ESTER
  • Indazole-6-boronic acid pinacol ester
  • 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]oxazole
  • 1,4-Difluoro-2-(isocyanatomethyl)-5-nitrobenzene
  • 2-Bromo-2-methylpropyl 2-propoxyacetate
  • 1-[(5-Azido-3-iodo-2,4-dimethylphenyl)methyl]piperazine
  • 2-[3-(aminomethyl)-2,2-dimethylcyclopropyl]-4-fluoro-N,N-dimethylaniline
  • 1-(4-Ethynylphenyl)cyclopropane-1-carbaldehyde
  • 3-Amino-1-(2-fluoro-4-nitrophenyl)propan-1-ol
  • rac-tert-butyl (3R,4S)-3-hydroxy-4-(2-methylthiophen-3-yl)pyrrolidine-1-carboxylate
  • 2-({1-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]cyclobutyl}formamido)-4,4,4-trifluorobutanoic acid
  • 2-Amino-7-(2-bromoethyl)-1,7-dihydro-6H-purin-6-one
  • 2-(Bromodifluoromethyl)-1,2-dimethylcyclopentan-1-ol
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