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??-2-?????

??-2-?????
??-2-????? ??? ???
?? ??:
1477-50-5
???:
??-2-?????
???(??):
??-2-?????
???:
Indole-2-carboxylic acid
???(??):
1H-INDOLE-2-CARBOXYLIC ACID;2-INDOLECARBOXYLIC ACID;NSC 16598;e-2-carboxyL;AKOS JY2082713;2-CARBOXYINDOLE;Indol-2-carbonsure;Indole-2-carboxylic;2-Carboxy-1H-indole;TIMTEC-BB SBB003953
CBNumber:
CB7728231
???:
C9H7NO2
??? ??:
161.16
MOL ??:
1477-50-5.mol
MSDS ??:
SDS

??-2-????? ??

???
202-206 °C(lit.)
?? ?
287.44°C (rough estimate)
??
1.2480 (rough estimate)
???
1.5050 (estimate)
?? ??
Keep in dark place,Sealed in dry,Room Temperature
???
Soluble in clear yellow solution 5% in ethanol, dimethyl sulfoxide and methanol.
?? ?? (pKa)
4.44±0.30(Predicted)
??? ??
??? ?? ?? ??
??
????? ???, ????
BRN
124132
CAS ??????
1477-50-5(CAS DataBase Reference)
NIST
Indole-2-carboxylic acid(1477-50-5)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? Xn,Xi
?? ???? ?? 36/37/38-21/22
????? 22-24/25
WGK ?? 3
RTECS ?? NK7882812
?? ?? IRRITANT
HS ?? 29339990
????(GHS): GHS hazard pictograms
?? ?: Warning
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H301 ??? ??? ?? ?? ?? - ?? ?? 3 ?? GHS hazard pictograms P264, P270, P301+P310, P321, P330,P405, P501
H311 ??? ???? ??? ?? ?? ?? - ?? ?? 3 ?? GHS hazard pictograms P280, P302+P352, P312, P322, P361,P363, P405, P501
H315 ??? ??? ??? ????? ?? ????? ?? 2 ?? GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 ?? ?? ??? ??? ?? ? ?? ?? ??? ?? ?? 2A ?? GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 ?? ???? ??? ? ?? ?? ???? ?? - 1? ??;???? ?? ?? 3 ?? GHS hazard pictograms
??????:
P261 ??·?·??·???·??·...·????? ??? ????.
P280 ????/???/???/?????? ?????.
P305+P351+P338 ?? ??? ? ?? ?? ???? ????. ???? ?????? ?????. ?? ????.
P405 ???? ?????.
NFPA 704
0
2 0

??-2-????? MSDS


Indole-2-carboxylic acid

??-2-????? C??? ??, ??, ??

??? ??

Yellow Crystalline Powder

??

• ;Reactant for total synthesis of (±)-dibromophakellin and analogs1• ;Reactant for synthesis of the pyrrolizidine alkaloid (±)-trachelanthamidine2• ;Reactant for stereoselective preparation of renieramycin G analogs3• ;Reactant for preparation of spirooxoindolepyrrolidines via reduction of indole-2-carboxylic acid followed by oxidation, condensation, reduction, amidation and Kharasch radical cyclization4• ;Reactant for Pd-catalyzed cyclization5• ;Reactant for preparation of N,N′-(pentane)diylbis[indolecarboxamide] and N,N′-[phenylenebis(

Synthesis Reference(s)

Tetrahedron Letters, 33, p. 7961, 1992 DOI: 10.1016/S0040-4039(00)74789-7

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