6-Benzyloxyindole
- Product Name
- 6-Benzyloxyindole
- CAS No.
- 15903-94-3
- Chemical Name
- 6-Benzyloxyindole
- Synonyms
- NSC 92538;6-BENZYLOXYINDOLE;6-Benzloxy-indole;NH6-Benzyloxyindole;6-BENZYLOXYINDOLE 97%;6-phenylMethoxyindole;6-Benzyloxyindole >6-Benzyloxyindole ,98%;6-(Benzyloxy)-1H-indole;6-(Benzyloxy)-1H-indole 98%
- CBNumber
- CB2208336
- Molecular Formula
- C15H13NO
- Formula Weight
- 223.27
- MOL File
- 15903-94-3.mol
6-Benzyloxyindole Property
- Melting point:
- 116-119°C
- Boiling point:
- 411.6±20.0 °C(Predicted)
- Density
- 1.196±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- solubility
- Chloroform (Slightly), Diethyl Ether (Slightly), Ethanol (Slightly), Ethyl Aceta
- pka
- 17.17±0.30(Predicted)
- form
- crystalline
- color
- yellow to brown
- BRN
- 173319
- InChI
- InChI=1S/C15H13NO/c1-2-4-12(5-3-1)11-17-14-7-6-13-8-9-16-15(13)10-14/h1-10,16H,11H2
- InChIKey
- FPMICYBCFBLGOZ-UHFFFAOYSA-N
- SMILES
- N1C2=C(C=CC(OCC3=CC=CC=C3)=C2)C=C1
- CAS DataBase Reference
- 15903-94-3(CAS DataBase Reference)
Safety
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 22-24/25-36/37/39-26
- WGK Germany
- 3
- Hazard Note
- Irritant/Keep Cold
- HS Code
- 29339990
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H226Flammable liquid and vapour
H315Causes skin irritation
H319Causes serious eye irritation
- Precautionary statements
-
P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
P233Keep container tightly closed.
P240Ground/bond container and receiving equipment.
P241Use explosion-proof electrical/ventilating/lighting/…/equipment.
P242Use only non-sparking tools.
P243Take precautionary measures against static discharge.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P332+P313IF SKIN irritation occurs: Get medical advice/attention.
P337+P313IF eye irritation persists: Get medical advice/attention.
P370+P378In case of fire: Use … for extinction.
P403+P235Store in a well-ventilated place. Keep cool.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- B5131
- Product name
- 6-Benzyloxyindole
- Purity
- crystalline
- Packaging
- 250mg
- Price
- $74.1
- Updated
- 2023/06/20
- Product number
- B2809
- Product name
- 6-Benzyloxyindole
- Purity
- >98.0%(GC)
- Packaging
- 1g
- Price
- $72
- Updated
- 2025/07/31
- Product number
- B2809
- Product name
- 6-Benzyloxyindole
- Purity
- >98.0%(GC)
- Packaging
- 5g
- Price
- $217
- Updated
- 2025/07/31
- Product number
- B2809
- Product name
- 6-Benzyloxyindole
- Purity
- >98.0%(GC)
- Packaging
- 25g
- Price
- $767
- Updated
- 2025/07/31
- Product number
- B285945
- Product name
- 6-Benzyloxyindole
- Packaging
- 50mg
- Price
- $50
- Updated
- 2021/12/16
6-Benzyloxyindole Chemical Properties,Usage,Production
Chemical Properties
Colourless Crystalline Solid
Uses
Indole derivative, as antiviral and antitumor agent
Uses
- Reactant for enantioselective synthesis of quaternary carbon-containing 3-(3-indolyl)isoindolin-1-ones
- Reactant for Friedel-Crafts alkylation reactions with hydroxyisoindolinones
- Reactant for direct and regioselective synthesis of β-heteroarylated ketones
- Reactant for preparation of hepatitis C virus (HCV) inhibitors
- Reactant for preparation of protein kinase C (PKC) inhibitors
- Reactant for preparation of indol-3-yl tetramethylcyclopropyl ketones as CB2 cannabinoid receptor ligands
Synthesis
153805-86-8
2380-86-1
15903-94-3
The compound (CAS: 153805-86-8) was used as starting material and synthesized by a method similar to Example 32. The specific operation was as follows: 5% rhodium/carbon powder was added to the reaction system as a catalyst, and the metal compounds ferrous acetate (II), nickel nitrate (II) or cobalt acetylacetonate (III) were introduced as co-catalysts. 5-Benzyloxy-2-(2-pyrrolidinylvinyl)nitrobenzene was used as the substrate for the reduction reaction. Upon completion of the reaction, as shown in Table 6, the yield of 6-benzyloxyindole was significantly increased and the by-product yield of 6-hydroxyindole was decreased when the reducing agent of the present invention was used as compared to the counterpart 5.
References
[1] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 39-40
[2] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 39-40
[3] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 39-40
[4] Patent: EP1541582, 2005, A1. Location in patent: Page/Page column 39-40
[5] Organic Process Research and Development, 2006, vol. 10, # 6, p. 1178 - 1183
6-Benzyloxyindole Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 6-Benzyloxyindole manufacturers
- Product
- 6-Benzyloxyindole 15903-94-3
- Price
- US $1.00/kg
- Min. Order
- 1kg
- Purity
- 99%
- Supply Ability
- 10 m
- Release date
- 2024-11-29
- Product
- 6-Benzyloxyindole in stock Factory 15903-94-3
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- TOP 3 Factory in China
- Supply Ability
- Top 3 largest production capacity Factory
- Release date
- 2019-04-03
- Product
- 6-Benzyloxyindole 15903-94-3
- Price
- US $1.00/kg
- Min. Order
- 1kg
- Purity
- 95%-99%
- Supply Ability
- as request
- Release date
- 2018-12-24