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1-(5-chloro-2-ethoxy-3-iodo-4-methylphenyl)ethanone is a complex organic chemical compound characterized by a phenyl ring with chloro, ethoxy, and iodo substituents, along with a ketone functional group. 1-(5-chloro-2-ethoxy-3-iodo-4-methylphenyl)ethanone may serve as a versatile building block for the synthesis of more complex organic molecules, with potential applications across various sectors contingent upon its reactivity, stability, and toxicity, which are yet to be fully determined through further research and testing.

1382996-91-9

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1382996-91-9 Usage

Uses

Used in Pharmaceutical Industry:
1-(5-chloro-2-ethoxy-3-iodo-4-methylphenyl)ethanone is used as a synthetic intermediate for the development of pharmaceutical compounds, leveraging its unique molecular structure to create new drugs with potential therapeutic applications.
Used in Agricultural Industry:
In the agricultural sector, 1-(5-chloro-2-ethoxy-3-iodo-4-methylphenyl)ethanone may be utilized as a precursor in the synthesis of agrochemicals, such as pesticides or herbicides, due to its potential to form stable and effective molecules for crop protection.
Used in Industrial Applications:
1-(5-chloro-2-ethoxy-3-iodo-4-methylphenyl)ethanone could be employed as a key component in the production of specialty chemicals or materials in the industrial sector, where its specific properties might contribute to the development of innovative products with unique characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 1382996-91-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,2,9,9 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1382996-91:
(9*1)+(8*3)+(7*8)+(6*2)+(5*9)+(4*9)+(3*6)+(2*9)+(1*1)=219
219 % 10 = 9
So 1382996-91-9 is a valid CAS Registry Number.

1382996-91-9Downstream Products

1382996-91-9Relevant academic research and scientific papers

INCB050465 (Parsaclisib), a Novel Next-Generation Inhibitor of Phosphoinositide 3-Kinase Delta (PI3Kδ)

Yue, Eddy W.,Li, Yun-Long,Douty, Brent,He, Chunhong,Mei, Song,Wayland, Brian,Maduskuie, Thomas,Falahatpisheh, Nikoo,Sparks, Richard B.,Polam, Padmaja,Zhu, Wenyu,Glenn, Joseph,Feng, Hao,Zhang, Ke,Li, Yanlong,He, Xin,Katiyar, Kamna,Covington, Maryanne,Feldman, Patricia,Shin, Niu,Wang, Kathy He,Diamond, Sharon,Li, Yu,Koblish, Holly K.,Hall, Leslie,Scherle, Peggy,Yeleswaram, Swamy,Xue, Chu-Biao,Metcalf, Brian,Combs, Andrew P.,Yao, Wenqing

, p. 1554 - 1560 (2019/11/11)

A medicinal chemistry effort focused on identifying a structurally diverse candidate for phosphoinositide 3-kinase delta (PI3Kδ) led to the discovery of clinical candidate INCB050465 (20, parsaclisib). The unique structure of 20 contains a pyrazolopyrimidine hinge-binder in place of a purine motif that is present in other PI3Kδinhibitors, such as idelalisib (1), duvelisib (2), and INCB040093 (3, dezapelisib). Parsaclisib (20) is a potent and highly selective inhibitor of PI3Kδwith drug-like ADME properties that exhibited an excellent in vivo profile as demonstrated through pharmacokinetic studies in rats, dogs, and monkeys and through pharmacodynamic and efficacy studies in a mouse Pfeiffer xenograft model.

IMIDAZO [1,5-A] PYRAZINE DERIVATIVES AS PI3Kdelta INHIBITORS

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, (2018/06/30)

Disclosed is a compound of Formula (I), or a stereoisomer thereof, or a pharmaceutically acceptable salt thereof, and pharmaceutical compositions comprising thereof. Also disclosed is a method of treating PI3Kδ related disorders or diseases by using the c

USE OF PYRAZOLOPYRIMIDINE DERIVATIVES FOR THE TREATMENT OF PI3K-DELTA RELATED DISORDERS

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, (2014/09/16)

The present application provides methods of treating PI3Kδ related disorders using compounds of Formula I: or pharmaceutically acceptable salts thereof.

HETEROCYCLYLAMINES AS PI3K INHIBITORS

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, (2013/03/26)

The present invention provides heterocyclylamine derivatives of Formula I: wherein the variables are defined herein, that modulate the activity of phosphoinositide 3-kinases (PI3Ks) and are useful in the treatment of diseases related to the activity of PI3Ks including, for example, inflammatory disorders, immune-based disorders, cancer, and other diseases.

N-(1-(SUBSTITUTED-PHENYL)ETHYL)-9H-PURIN-6-AMINES AS PI3K INHIBITORS

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, (2012/06/30)

The present invention provides N-(1-(substituted-phenyl)ethyl)-9H-purin-6-amines derivatives that modulate the activity of phosphoinositide 3-kinases (PI3Ks) and are useful in the treatment of diseases related to the activity of PI3Ks including, for examp

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