192189-10-9 Usage
Description
3-IODO-5-METHOXYINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is a chemical compound with the molecular formula C17H19INO3, belonging to the indole class of heterocyclic aromatic organic compounds. It is characterized by the presence of an iodo and methoxy substituent, along with a tert-butyl ester group that provides stability and protection for the indole core. 3-IODO-5-METHOXYINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is known for its unique properties and reactivity, making it a valuable intermediate in organic synthesis.
Uses
Used in Organic Chemistry:
3-IODO-5-METHOXYINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique properties and reactivity.
Used in Pharmaceutical Industry:
3-IODO-5-METHOXYINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is used as an intermediate in the development of new pharmaceutical compounds, leveraging its versatility and functionality to create novel drug candidates.
Used in Agrochemical Industry:
3-IODO-5-METHOXYINDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER is used as a key component in the synthesis of agrochemicals, contributing to the development of innovative and effective products for agricultural applications.
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
192189-10-9Relevant 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
Harmful:;
