2-Phenylindole_ CAS NO.948-65-2

Min.Order Quantity:: 1 Kilogram

Purity:: 99.0%

Port:: SHANGHAI

Payment Terms:: L/C,D/A,D/P,T/T,MoneyGram,Other

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Product Details

Keywords

2-Phenylindole
948-65-2
2-Phenylindole

Quick Details

ProName: 2-Phenylindole_
CasNo: 948-65-2
Molecular Formula: C14H11N
Appearance: off-white to beige or slightly green p...
Application: For Organic Synthesis use
DeliveryTime: PROMPT
PackAge: IN 25kg drums
Port: SHANGHAI
ProductionCapacity: 10 Metric Ton/Month
Purity: 99.0%
Storage: In Room Temperature
Transportation: As Per MSDS
LimitNum: 1 Kilogram
Heavy metal: N/A
Grade: Industrial Grade,Food Grade,Pharma Gra...
N/A: N/A

Superiority

2-phenylindole basic information

product name:	2-phenylindole
synonyms:	1h-indole,2-phenyl-;2-phenyl-1h-indol;2-phenyl-indol;alpha-phenylindole;indole, 2-phenyl-;-phenylindole;stabilizer i;stabilizeri
cas:	948-65-2
mf:	c14h11n
mw:	193.24
einecs:	213-436-3
product categories:	indole;heterocyclic compounds;indoles;simple indoles;building blocks;heterocyclic building blocks;building blocks;c13 to c27;chemical synthesis;heterocyclic building blocks;heterocycle-indole series;intermediates
mol file:	948-65-2.mol

Details

2-phenylindole chemical properties

mp	188-190 °c(lit.)
bp	250 °c10 mm hg(lit.)
fp	250°c/10mm
cas database reference	948-65-2(cas database reference)
nist chemistry reference	1h-indole, 2-phenyl-(948-65-2)
epa substance registry system	1h-indole, 2-phenyl-(948-65-2)

safety information

hazard codes	xi
risk statements	37/38-41
safety statements	26-39
wgk germany	3
rtecs	nm1272500

2-phenylindole usage and synthesis

chemical properties

off-white to beige or slightly green powder

usage

reactant for preparation of: • ;oxopyrrolidine analogs via iodine-catalyzed markovnikov addition1• ;tryptophan dioxygenase inhibitors pyridyl-ethenyl-indoles as potential anticancer immunomodulators2• ;organic light emitting diodes (oleds)3• ;anti inflammatory agents4• ;potential cyclooxygenase-1 (cox-1)/cyclooxygenase-2 (cox-2) inhibitors5• ;agents for cancer and malaria therapy6• ;antifungal and antibacterial agents7• ;fluorescent probes8reactant in:• ;difluorohydroxylation reactions†• ;mannich-type reactions†

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