3-(2-Hydroxyethyl)-1H-indol-5-ol

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Names

[ CAS No. ]:
154-02-9

[ Name ]:
3-(2-Hydroxyethyl)-1H-indol-5-ol

[Synonym ]:
1H-Indole-3-ethanol,5-hydroxy
INDOLE-3-ETHANOL,5-HYDROXY
5-hydroxytryprophol
5-Hydroxytryptophol
3-(2-hydroxy-ethyl)-indol-5-ol
3-(2-Hydroxyethyl)-1H-indol-5-ol
5-Hydroxyindole-3-ethanol
5-hydroxy-3-(2-hydroxyethyl)indole
5-Hydroxy-1H-indole-3-ethanol
1H-Indole-3-ethanol, 5-hydroxy-
MFCD00047197
5-hydroxy-3(2-hydroxyethyl)indole
3-(2-Hydroxy-aethyl)-indol-5-ol
Hydroxytryptophol
EINECS 205-820-4

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
435.2±30.0 °C at 760 mmHg

[ Molecular Formula ]:
C10H11NO2

[ Molecular Weight ]:
177.200

[ Flash Point ]:
217.0±24.6 °C

[ Exact Mass ]:
177.078979

[ PSA ]:
56.25000

[ LogP ]:
0.11

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

[ Index of Refraction ]:
1.718

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
NL8512500
CHEMICAL NAME :
Indole-3-ethanol, 5-hydroxy-
CAS REGISTRY NUMBER :
154-02-9
BEILSTEIN REFERENCE NO. :
0143517
LAST UPDATED :
199803
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C10-H11-N-O2
MOLECULAR WEIGHT :
177.22

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Ocular
DOSE :
1500 ug/kg
SEX/DURATION :
female 1 day(s) pre-mating
TOXIC EFFECTS :
Reproductive - Fertility - other measures of fertility
REFERENCE :
INJFA3 International Journal of Fertility. (Allen Press, 1041 New Hampshire, St., Lawrence, KS 66044) V.1- 1955- Volume(issue)/page/year: 19,117,1974

Safety Information

[ HS Code ]:
2933990090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 5-Hydroxyindole-3-acetic acid
  • 2-(5-phenylmethoxy-1H-indol-3-yl)ethanol
  • 5-benzyloxygramine
  • 5-benzyloxyindole-3-acetic acid

DownStream

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%

Related Compounds

  • 3-(2-hydroxyethyl)-4,6-dinitro-1H-indol-5-ol
  • 3-(2-amino-1-hydroxyethyl)-1H-indol-5-ol
  • 5-Hydroxy Tryptophol β-D-Glucuronide
  • 3-(2-aminoethyl)-1H-indol-5-ol,hexanedioic acid
  • 3-(2-aminoethyl)-1H-indol-5-ol,2-amino-3-methyl-4H-imidazol-5-one,sulfuric acid
  • 3-(2-aminoethyl)-1H-indol-5-ol,2,4,6-trinitrophenol
  • 2-hydroxybenzoic acid; N,N-diethylethanimidamide
  • 2-({1-[(furan-2-yl)methyl]-5-phenyl-1H-imidazol-2-yl}sulfanyl)acetonitrile
  • 2-(3-Chloro-5-(trifluoromethyl)pyridin-2-yl)isoindolin-1-imine hydrobromide
  • 1-(2-(N-Cyclohexyl-p-anisidino)ethyl)-1-methyl-piperidinium bromide
  • Phenylcarbamic acid 1-methyl-2-(3-oxo-1,2-benzisothiazol-2(3H)-yl)ethyl ester
  • 2,4-Diamino-5-[2-[4-[[2-(sulfooxy)ethyl]sulfonyl]phenyl]diazenyl]-3-[2-[2-sulfo-4-[[2-(sulfooxy)ethyl]sulfonyl]phenyl]diazenyl]benzenesulfonic acid
  • 1,1,1,2,3,4,4,4-Octafluoro-2-(1,1,2,2,3,3,3-heptafluoropropoxy)-3-[1,1,2,3,3,3-hexafluoro-2-(1,1,2,2,3,3,3-heptafluoropropoxy)propoxy]butane
  • N-[(1,5-Dimethyl-1H-pyrazol-4-YL)methyl]-1-methyl-1H-pyrazol-4-amine
  • 3-Propylbenzene-1-sulfonyl chloride
  • 3-N-Butylbenzenesulfonyl chloride
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