TERT-BUTYL 5-BROMO-1H-INDOLE-1-CARBOXYLATE

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Names

[ CAS No. ]:
182344-70-3

[ Name ]:
TERT-BUTYL 5-BROMO-1H-INDOLE-1-CARBOXYLATE

[Synonym ]:
MFCD02090067
Tert-Butyl 5-Bromoindole-1-Carboxylate

Chemical & Physical Properties

[ Density]:
1.37g/cm3

[ Boiling Point ]:
367.9ºC at 760mmHg

[ Melting Point ]:
56-57ºC(lit.)

[ Molecular Formula ]:
C13H14BrNO2

[ Molecular Weight ]:
296.16000

[ Flash Point ]:
176.3ºC

[ Exact Mass ]:
295.02100

[ PSA ]:
31.23000

[ LogP ]:
4.18700

[ Vapour Pressure ]:
1.33E-05mmHg at 25°C

[ Index of Refraction ]:
1.576

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 ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933990090

Synthetic Route

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

Structure-activity relationship analysis of the peptide deformylase inhibitor 5-bromo-1H-indole-3-acetohydroxamic acid.

ChemMedChem 4 , 261, (2009)

The lead compound 5-bromoindolyl-3-acetohydroxamic acid (10) was recently identified as a potent inhibitor of bacterial peptide deformylases (PDFs). The synthesis and associated activities of new vari...

Synthesis of heterocyclic allenes via palladium-catalyzed hydride-transfer reaction of propargylic amines.

J. Org. Chem. 70(6) , 2357-60, (2005)

[reaction: see text] Propargylic diisopropylamines containing heterocycles, which were prepared readily from heterocyclic bromides and propargyldiisopropylamine by the Sonogashira coupling reaction, u...


More Articles


Related Compounds

  • tert-Butyl 5-bromo-3-(cyanomethyl)-1H-indole-1-carboxylate
  • Tert-butyl 5-bromo-4-formyl-7-methyl-1H-indole-1-carboxylate
  • tert-Butyl 5-bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
  • TERT-BUTYL 5-(BENZYLOXY)-3-BROMO-1H-INDOLE-1-CARBOXYLATE
  • 1-Boc-5-Bromo-3-iodoindole
  • 1-BOC-5-BROMO-3-FORMYLINDOLE
  • 2-((Methylamino)methyl)propane-1,3-diol hydrochloride
  • CID 132398786
  • 7-Fluoro-2,3,4,5-tetrahydrobenzo[f][1,4]oxazepine hydrochloride
  • Lithium(1+) ion [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate
  • 4-Aminofuro[3,2-c]pyridine-2-carbonitrile hydrochloride
  • 4-(Methylsulfonimidoyl)phenol;hydrobromide
  • Methyl 2-chloro-1h-1,3-benzodiazole-6-carboxylate hydrochloride
  • (3aS,7aR)-2-(((9H-fluoren-9-yl)methoxy)carbonyl)-5-methyloctahydro-7aH-pyrrolo[3,4-c]pyridine-7a-carboxylic acid hydrochloride
  • 1-[(3-Bromo-2-fluorophenyl)methyl]pyrrolidin-2-one
  • N-Methyl-2-pyrazol-1-ylcyclopentan-1-amine;hydrochloride
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