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7-METHOXY-1-METHYL-D-TRYPTOPHAN ETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

655239-35-3

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655239-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 655239-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,5,2,3 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 655239-35:
(8*6)+(7*5)+(6*5)+(5*2)+(4*3)+(3*9)+(2*3)+(1*5)=173
173 % 10 = 3
So 655239-35-3 is a valid CAS Registry Number.

655239-35-3SDS

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-1-methylindol-3-yl)propanoate

1.2 Other means of identification

Product number -
Other names Na-methyl-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:655239-35-3 SDS

655239-35-3Relevant academic research and scientific papers

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

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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