5-METHOXYTRYPTOPHOL Chemical Properties

Boiling point:

326.97°C (rough estimate)

Density 

1.224

refractive index 

1.5220 (estimate)

storage temp. 

Sealed in dry,2-8°C

solubility 

Chloroform (Slightly), Methanol (Slightly)

form 

Viscous Liquid

pka

14.90±0.10(Predicted)

color 

Dark Yellow to Very Dark Brown

CAS DataBase Reference

712-09-4(CAS DataBase Reference)

Safety Information

Hazard Codes 

Xi

WGK Germany 

3

RTECS 

NL8513000

HazardClass 

IRRITANT

HS Code 

2933998090

MSDS

• Language:English Provider:SigmaAldrich

5-METHOXYTRYPTOPHOL Usage And Synthesis

Description

5-methoxy Tryptophol (5-MTOH) is a natural indole that is produced by the pineal gland. It is a product of melatonin metabolism that may be biologically active. The levels of 5-MTOH in plasma vary in a diurnal pattern in rodents and humans.

Uses

5-Methoxytryptophol is a compound known to play a significant role in bone metabolism. 5-Methoxytryptophol can inhibit osteoclastogenesis and promote osteoblast differentiation.

Definition

ChEBI: 5-Methoxytryptophol is a member of indoles.

Synthesis

General procedure for the synthesis of 5-methoxychromanol from 2,3-dihydrofuran and 4-methoxyphenylhydrazine hydrochloride: 1. dissolve 4-methoxyphenylhydrazine hydrochloride (1.214 g, 6.95 mmol) in a mixture of 10 mL of 0.72 M H2SO4 and 10 mL of DMA and heat to 55°C. 2. 2,3-dihydrofuran (0.525 mL, 6.95 mmol) was added slowly over 2 minutes. 3. the reaction mixture was stirred at 55 °C for 2 h and subsequently cooled to room temperature. 4. The reaction mixture was extracted with isopropyl acetate (2 x 25 mL). 5. The organic layers were combined and washed sequentially with H2O (3 x 20 mL) and saturated NaCl solution (1 x 20 mL). 6. The organic layer was dried with Na2SO4, filtered and concentrated. 7. The crude product was purified by fast chromatography (eluent: 50:50 ethyl acetate/hexane) to afford 3-(2-hydroxyethyl)-5-methoxy-1H-indole (5-methoxytryptophan) (11) as an orange-red oil.

IC 50

Human Endogenous Metabolite

References

[1] Angewandte Chemie - International Edition, 2018, vol. 57, # 23, p. 6888 - 6891
[2] Angew. Chem., 2018, vol. 130, # 23, p. 7004 - 7007,4
[3] Organic Letters, 2017, vol. 19, # 7, p. 1504 - 1507
[4] Tetrahedron Letters, 2013, vol. 54, # 40, p. 5489 - 5491
[5] Advanced Synthesis and Catalysis, 2010, vol. 352, # 2-3, p. 363 - 367

5-METHOXYTRYPTOPHOL(712-09-4)Related Product Information

• Acemetacin
• PROGLUMETACIN MALEATE
• 5-Methoxyindole-3-acetic acid
• Indometacin
• Talmetacin
• zidometacin
• 5-METHOXYTRYPTOPHOL
• INDOMETHACIN SODIUM SALT TRIHYDRATE
• METHYL 5-BENZYLOXYINDOLE-3-ACETATE
• cinmetacin
• Indorenate
• 5-METHOXY-2-METHYL-3-INDOLEACETIC ACID
• 5-BENZYLOXYINDOLE-3-ACETIC ACID
• 5-BENZYLOXYINDOLE-3-GLYOXYLIC ACID ETHYL ESTER
• 2-(5-BENZYLOXY-1H-INDOL-3-YL)-ETHANOL
• niometacin
• 6-methoxytryptophol
• carbazomycin H