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1H-Indole-1,2-dicarboxylic acid, 5,6,7-trimethoxy-, 2-methyl 1-(phenylmethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

556038-54-1

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556038-54-1 Usage

Molecular class

Indole derivatives

Molecular weight

389.4

Structure

1H-Indole-1,2-dicarboxylic acid with three methoxy groups on the indole ring, a methyl group at the 2-position, and a phenylmethyl group at the 1-position.

Properties

Potential applications in medicinal chemistry and pharmaceutical research due to the indole core structure found in many biologically active molecules. Further research is needed to determine specific properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 556038-54-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,6,0,3 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 556038-54:
(8*5)+(7*5)+(6*6)+(5*0)+(4*3)+(3*8)+(2*5)+(1*4)=161
161 % 10 = 1
So 556038-54-1 is a valid CAS Registry Number.

556038-54-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyloxycarbonyl-5,6,7-trimethoxy-1H-indole-2-carboxylic acid methyl ester

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:556038-54-1 SDS

556038-54-1Relevant academic research and scientific papers

Total synthesis of the duocarmycins

Yamada, Ken,Kurokawa, Toshiki,Tokuyama, Hidetoshi,Fukuyama, Tohru

, p. 6630 - 6631 (2007/10/03)

The total synthesis of (+)-duocarmycin A and SA through a common indoline intermediate is described. The key reactions include selective lithiation of a 2,6-dibromoiodobenzene derivative and diastereoselective addition to a chiral nitroalkene, copper-mediated aryl amination, and addition of aryllithium to azlactones. Copyright

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