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655240-16-7

7-METHOXY-D-TRYPTOPHAN ETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 655240-16-7 Structure

  • Basic information

    1. Product Name: 7-METHOXY-D-TRYPTOPHAN ETHYL ESTER
    2. Synonyms: 7-METHOXY-D-TRYPTOPHAN ETHYL ESTER
    3. CAS NO:655240-16-7
    4. Molecular Formula: C14H18N2O3
    5. Molecular Weight: 262.3
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 655240-16-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 7-METHOXY-D-TRYPTOPHAN ETHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-METHOXY-D-TRYPTOPHAN ETHYL ESTER(655240-16-7)
    11. EPA Substance Registry System: 7-METHOXY-D-TRYPTOPHAN ETHYL ESTER(655240-16-7)

  • 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: 655240-16-7(Hazardous Substances Data)

655240-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 655240-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,5,2,4 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 655240-16:
(8*6)+(7*5)+(6*5)+(5*2)+(4*4)+(3*0)+(2*1)+(1*6)=147
147 % 10 = 7
So 655240-16-7 is a valid CAS Registry Number.

655240-16-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (2R)-2-amino-3-(7-methoxy-1H-indol-3-yl)propanoate

1.2 Other means of identification

Product number -
Other names 7-METHOXY-D-TRYPTOPHAN ETHYL ESTER

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:655240-16-7 SDS

655240-16-7Downstream Products

655240-16-7Relevant articles and documents

General approach for the synthesis of 12-methoxy-substituted sarpagine indole alkaloids including (-)-12-methoxy-Nb-methylvoachalotine, (+)-12-methoxy-Na-methylvellosimine, (+)-12-methoxyaffinisine, and (-)-fuchsiaefoline

Zhou, Hao,Liao, Xuebin,Yin, Wenyuan,Ma, Jun,Cook, James M.

, p. 251 - 259 (2007/10/03)

The enantiospecific synthesis of 7-methoxy-D-tryptophan ethyl ester was completed by combination of the Larock heteroannulation process with a Schoellkopf-based chiral auxiliary in good yield. This ester was then employed in the first regiospecific, stere

Synthesis of optically active ring-A substituted tryptophans as IDO inhibitors

Li, Xiaoyan,Yin, Wenyuan,Sarma, P.V.V. Srirama,Zhou, Hao,Jun Ma,Cook, James M.

, p. 8569 - 8573 (2007/10/03)

The first synthesis of optically active 7-methoxy-d-tryptophan as well as other ring-A substituted tryptophans is described.

Regiospecific, Enantiospecific Total Synthesis of the 12-Alkoxy- Substituted Indole Alkaloids, (+)-12-Methoxy-Na-methylvellosimine, (+)-12-Methoxyaffinisine, and (-)-Fuchsiaefoline

Zhou, Hao,Liao, Xuebin,Cook, James M.

, p. 249 - 252 (2007/10/03)

(Matrix presented) The enantiospecific synthesis of 7-methoxy-D-tryptophan was completed by combination of the Larock heteroannulation process with a Schoellkopf-based chiral auxiliary in good yield. This ester was then employed in the first total synthes

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