Benzyloxy-5 indole

Name	5-Benzyloxyindole
Synonyms	bredreck`s 5-Benzyloxyindole 5-benzyloxy-indol 5-BENZYLOXYINDOLE Benzyloxy-5 indole TIMTEC-BB SBB003331 BENZYLOXYINDOLE(5-) Benzyloxyindole(5-) 5-BENZYLOXY-1H-INDOLE 5-Benzyloxy-1H-Indole Indole, 5-(benzyloxy)- 5-(Phenylmethoxy)-1H-indole bis-hydroxyethyl-p-aniline sulphate
CAS	1215-59-4
EINECS	214-930-1
InChI	InChI=1/C15H13NO/c1-2-4-12(5-3-1)11-17-14-6-7-15-13(10-14)8-9-16-15/h1-10,16H,11H2

Molecular Formula	C15H13NO
Molar Mass	223.27
Density	1.0707 (rough estimate)
Melting Point	100-104 °C (lit.)
Boling Point	364.56°C (rough estimate)
Flash Point	148.9°C
Solubility	ethanol: may be hazy yellow
Vapor Presure	1.31E-06mmHg at 25°C
Appearance	White powder
Color	white to light yellow
Exposure Limit	ACGIH: TWA 20 ppmOSHA: Ceiling 300 ppm; TWA 200 ppmNIOSH: IDLH 500 ppm; TWA 100 ppm(375 mg/m3); STEL 150 ppm(560 mg/m3)
BRN	173532
pKa	16.63±0.30(Predicted)
Storage Condition	2-8°C
Refractive Index	1.5500 (estimate)
MDL	MFCD00005676
Physical and Chemical Properties	Melting point 96-102°C

Hazard Symbols	Xi - Irritant
Risk Codes	36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S24/25 - Avoid contact with skin and eyes. S22 - Do not breathe dust.
WGK Germany	3
RTECS	NL4850000
FLUKA BRAND F CODES	8-10
HS Code	29339990
Hazard Class	IRRITANT

NIST chemical information	Information provided by: webbook.nist.gov (external link)
Introduction	5-benzyloxyindole can be used as an intermediate in pharmaceutical synthesis. It can be prepared by four-step reaction from m-cresol. 5-benzyloxy indole can be used to prepare (L)-5-hydroxytryptophan. 5-HTP (5-hydroxytryptophan) is a pure natural herbal prescription with a calming effect. It is a precursor of a hormone called serotonin in the human body. It can help people produce this hormone in the body and achieve balance in their bodies.
Application	5-benzyloxyindole is an indole organic compound, which can be used for regional and stereoselective morpholine catalysis; under mild reaction conditions, under the silicic acid-palladium catalytic system, it is used to protect the group's selective debenzylation reagent; it is used for metal-free Friedel-Crafts alkylation reagent; reagents for the preparation of protein kinase (PKC) inhibitors; Reagents for the preparation of indole/quinoline thiohydroxylamide derivatives.

Last Update：2024-04-09 02:00:06

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