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Diethyl [(2-methyl-1H-indol-3-yl)methyl]propanedioate is a synthetic chemical compound with the molecular formula C17H21NO4. It is a derivative of the heterocyclic indole, which is commonly found in plant alkaloids. diethyl [(2-methyl-1H-indol-3-yl)methyl]propanedioate is characterized by its colorless liquid form, a faint sweet odor, and solubility in organic solvents such as ethanol and ether. Its versatile reactivity and potential biological activity make it a valuable intermediate in the synthesis of pharmaceutical drugs and other organic compounds.

6637-12-3

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6637-12-3 Usage

Uses

Used in Pharmaceutical Industry:
Diethyl [(2-methyl-1H-indol-3-yl)methyl]propanedioate is used as a chemical intermediate for the synthesis of various pharmaceutical drugs. Its unique structure and reactivity allow for the creation of new drug molecules with potential therapeutic applications.
Used in Chemical Industry:
In the chemical industry, diethyl [(2-methyl-1H-indol-3-yl)methyl]propanedioate serves as a key component in the production of other organic compounds. Its versatility in chemical reactions enables the development of novel chemical entities for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6637-12-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6637-12:
(6*6)+(5*6)+(4*3)+(3*7)+(2*1)+(1*2)=103
103 % 10 = 3
So 6637-12-3 is a valid CAS Registry Number.

6637-12-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 2-[(2-methyl-1H-indol-3-yl)methyl]propanedioate

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 -
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More Details:6637-12-3 SDS

6637-12-3Downstream Products

6637-12-3Relevant academic research and scientific papers

5-(Cyano)dibenzothiophenium Triflate: A Sulfur-Based Reagent for Electrophilic Cyanation and Cyanocyclizations

Li, Xiangdong,Golz, Christopher,Alcarazo, Manuel

supporting information, p. 9496 - 9500 (2019/06/27)

The synthesis of 5-(cyano)dibenzothiophenium triflate 9, prepared by activation of dibenzo[b,d]thiophene-5-oxide with Tf2O and subsequent reaction with TMSCN is reported, and its reactivity as electrophilic cyanation reagent evaluated. The scalable preparation, easy handling and broad substrate scope of the electrophilic cyanation promoted by 9, which includes amines, thiols, silyl enol ethers, alkenes, electron rich (hetero)arenes and polyaromatic hydrocarbons, illustrate the synthetic potential of this reagent. Importantly, Lewis acid activation of the reagent is not required for the transfer process. We additionally report herein biomimetic cyanocyclization cascade reactions, which are not promoted by typical electrophilic cyanation reagents, demonstrating the superior ability of 9 to trigger challenging transformations.

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