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192189-10-9

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192189-10-9 Usage

General Description

3-Iodo-5-methoxyindole-1-carboxylic acid tert-butyl ester is a chemical compound with the molecular formula C17H19INO3. It is a derivative of indole, a heterocyclic aromatic organic compound. 3-IODO-5-METHOXYINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is commonly used in the field of organic chemistry for its unique properties and reactivity. It is often employed as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Its tert-butyl ester group also provides stability and protection for the indole core, making it a valuable intermediate in organic synthesis. Additionally, the presence of the iodo and methoxy substituents adds further versatility and functionality to the molecule, making it a valuable tool in the development of new chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 192189-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,1,8 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 192189-10:
(8*1)+(7*9)+(6*2)+(5*1)+(4*8)+(3*9)+(2*1)+(1*0)=149
149 % 10 = 9
So 192189-10-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H16INO3/c1-14(2,3)19-13(17)16-8-11(15)10-7-9(18-4)5-6-12(10)16/h5-8H,1-4H3

192189-10-9SDS

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 tert-butyl 3-iodo-5-methoxyindole-1-carboxylate

1.2 Other means of identification

Product number -
Other names OR1713

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:192189-10-9 SDS

192189-10-9Relevant articles and documents

COMPOUNDS AND METHOD OF USE

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Paragraph 1209, (2019/09/06)

This present disclosure relates to compounds with ferroptosis inducing activity, a method of treating a subject with cancer with the compounds, and combination treatments with a second therapeutic agent.

One-pot synthesis of diazine-bridged bisindoles and concise synthesis of the marine alkaloid hyrtinadine A

Tasch, Boris O. A.,Merkul, Eugen,Mueller, Thomas J. J.

supporting information; experimental part, p. 4532 - 4535 (2011/10/03)

Diazine-bridged bisindoles are readily obtained from N-Bocprotected 3-iodoindoles and 3-iodo-7-azaindole in a pseudo three-component reaction involving a one-pot Masuda borylation-Suzuki arylation sequence. Some of the title com-pounds display promising c

Amino-zinc-ene-enolate cyclization: A short access to cis-3-substituted prolino-homotryptophane derivatives

Mothes, Celine,Lavielle, Solange,Karoyan, Philippe

, p. 6706 - 6710 (2008/12/22)

(Chemical Equation Presented) Proline chimeras are useful tools for medicinal chemistry and/or biological applications. The asymmetric synthesis of cis-3-substituted prolines can be easily achieved via amino-zinc-ene-enolate cyclization followed by transm

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