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6127-51-1

O-acetyl-5-methoxytryptophenol is a chemical compound derived from tryptophan, an essential amino acid. It is characterized by the presence of an acetyl group (an acetate ion) attached to the oxygen atom of the hydroxyl group, and a methoxy group (a methyl ether) attached to the 5th carbon of the tryptophan molecule. O-acetyl-5-methoxytryptophenol is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as an intermediate in the synthesis of other compounds. Its structure and properties make it a subject of study for understanding the effects of functional group modifications on the behavior of tryptophan derivatives.

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  • 6127-51-1 Structure

  • Basic information

    1. Product Name: O-acetyl-5-methoxytryptophenol
    2. Synonyms: O-acetyl-5-methoxytryptophenol
    3. CAS NO:6127-51-1
    4. Molecular Formula: C13H15 N O3
    5. Molecular Weight: 233.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6127-51-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 399.5°C at 760 mmHg
    3. Flash Point: 195.4°C
    4. Appearance: /
    5. Density: 1.195g/cm3
    6. Vapor Pressure: 1.36E-06mmHg at 25°C
    7. Refractive Index: 1.589
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: O-acetyl-5-methoxytryptophenol(CAS DataBase Reference)
    11. NIST Chemistry Reference: O-acetyl-5-methoxytryptophenol(6127-51-1)
    12. EPA Substance Registry System: O-acetyl-5-methoxytryptophenol(6127-51-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 6127-51-1(Hazardous Substances Data)

6127-51-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6127-51-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,2 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6127-51:
(6*6)+(5*1)+(4*2)+(3*7)+(2*5)+(1*1)=81
81 % 10 = 1
So 6127-51-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NO3/c1-9(15)17-6-5-10-8-14-13-4-3-11(16-2)7-12(10)13/h3-4,7-8,14H,5-6H2,1-2H3

6127-51-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tetramethyl 3-(2-methylpropyl)cyclopropane-1,1,2,2-tetracarboxylate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6127-51-1 SDS

6127-51-1Relevant articles and documents

Synthesis of 1-indolyl substituted β-carboline natural products and discovery of antimalarial and cytotoxic activities

Liew, Lydia P.P.,Fleming, Jessica M.,Longeon, Arlette,Mouray, Elisabeth,Florent, Isabelle,Bourguet-Kondracki, Marie-Lise,Copp, Brent R.

, p. 4910 - 4920 (2014)

A series of 1-indolyl substituted β-carbolines including the natural products hyrtiosulawesine, pityriacitrin and pityriacitrin B were prepared via Pictet-Spengler condensation - oxidation strategy from the corresponding indolyl-acetaldehydes and substituted tryptamines. Efforts to prepare the C-1 methylene-linked β-carboline analogues for structure-activity relationship studies were unsuccessful. Biological evaluation revealed two analogues (5 and 41) to exhibit weak inhibition of phospholipase A2 (IC50 171 and 131 μM, respectively), two to act as antioxidants (3 and 43), and 12 analogues with activity towards a chloroquine-resistant strain (FcB1) of Plasmodium falciparum (IC50 1.0-23 μM). Testing against a panel of 60 human tumour cell lines revealed a general lack of cytotoxic effect for most of the compounds with the exception of β-carboline 42 exhibiting modest antileukaemic activity towards the HL-60(TB) cell line (LC50 4.2 μM). In addition, two novel structures (30 and 32) resulting from aldol condensation followed by Pictet-Spengler cyclisation displayed cytotoxicity with pronounced subpanel specificities towards colon cancer (COLO 205 and HCC-2998) cell lines.

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