What is the (E)-1-benzhydryl-4-cinnamylpiperazine?

(E)-1-benzhydryl-4-cinnamylpiperazine is , while it's Molecular Formula is C 26 H 28 N 2 . Used in Pharmaceutical Industry: (E)-1-benzhydryl-4-cinnamylpiperazine is used as a serotonin reuptake inhibitor for its potential role in managing neurological and psychiatric disorders. Its ability to inhibit the reuptake of serotonin can contribute to the treatment of conditions such as depression and anxiety. Used in Medicinal Chemistry Research: As a compound with potential antipsychotic properties, (E)-1-benzhydryl-4-cinnamylpiperazine is utilized in the development of new medications for the treatment of various psychiatric disorders. Its unique structure and pharmacological profile make it a valuable subject for research in medicinal chemistry.

What is the CAS number for (E)-1-benzhydryl-4-cinnamylpiperazine?

The CAS number of (E)-1-benzhydryl-4-cinnamylpiperazine is 16699-20-0.

What is (E)-1-benzhydryl-4-cinnamylpiperazine (16699-20-0) used for?

(E)-1-benzhydryl-4-cinnamylpiperazine is a piperazine derivative that features a benzhydryl group and a cinnamyl group attached to a six-membered piperazine ring in a trans configuration. This chemical compound is part of the piperazine class of organic compounds, known for their potential pharmacological properties.InChI:InChI=1/C26H28N2/c1-4-11-23(12-5-1)13-10-18-27-19-21-28(22-20-27)26(24-14-6-2-7-15-24)25-16-8-3-9-17-25/h1-17,26H,18-22H2/b13-10-

What is the (E)-1-benzhydryl-4-cinnamylpiperazine?

(E)-1-benzhydryl-4-cinnamylpiperazine is , while it's Molecular Formula is C 26 H 28 N 2 . Used in Pharmaceutical Industry: (E)-1-benzhydryl-4-cinnamylpiperazine is used as a serotonin reuptake inhibitor for its potential role in managing neurological and psychiatric disorders. Its ability to inhibit the reuptake of serotonin can contribute to the treatment of conditions such as depression and anxiety. Used in Medicinal Chemistry Research: As a compound with potential antipsychotic properties, (E)-1-benzhydryl-4-cinnamylpiperazine is utilized in the development of new medications for the treatment of various psychiatric disorders. Its unique structure and pharmacological profile make it a valuable subject for research in medicinal chemistry.

What is the CAS number for (E)-1-benzhydryl-4-cinnamylpiperazine?

The CAS number of (E)-1-benzhydryl-4-cinnamylpiperazine is 16699-20-0.

What is (E)-1-benzhydryl-4-cinnamylpiperazine (16699-20-0) used for?

(E)-1-benzhydryl-4-cinnamylpiperazine is a piperazine derivative that features a benzhydryl group and a cinnamyl group attached to a six-membered piperazine ring in a trans configuration. This chemical compound is part of the piperazine class of organic compounds, known for their potential pharmacological properties.InChI:InChI=1/C26H28N2/c1-4-11-23(12-5-1)13-10-18-27-19-21-28(22-20-27)26(24-14-6-2-7-15-24)25-16-8-3-9-17-25/h1-17,26H,18-22H2/b13-10-

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(E)-1-benzhydryl-4-cinnamylpiperazine

CAS：16699-20-0
purity：99%

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Reputable factory supply (E)-1-benzhydryl-4-cinnamylpiperazine 16699-20-0 in stock with high standard

Molecular Formula: C₂₆H₂₈N₂
Molecular Weight: 368.522
Vapor Pressure: 1.74E-10mmHg at 25°C
Boiling Point: 509.2°Cat760mmHg
Flash Point: 229.8°C
PSA： 6.48000
Density: 1.093g/cm³
LogP: 4.98280

(E)-1-benzhydryl-4-cinnamylpiperazine(Cas 16699-20-0) Usage

General Description

(E)-1-benzhydryl-4-cinnamylpiperazine is a chemical compound that belongs to the class of piperazines, which are organic compounds that contain a six-membered ring with two nitrogen atoms and four carbon atoms. This specific compound is a piperazine derivative that contains a benzhydryl group and a cinnamyl group, with the piperazine ring being in a trans configuration. It has been studied for its potential pharmacological properties, including its activity as a serotonin reuptake inhibitor and its potential as an antipsychotic agent. (E)-1-benzhydryl-4-cinnamylpiperazine has also been investigated for its potential use in the treatment of various neurological and psychiatric disorders. The compound's chemical structure and properties make it an interesting target for medicinal chemistry research.

InChI:InChI=1/C26H28N2/c1-4-11-23(12-5-1)13-10-18-27-19-21-28(22-20-27)26(24-14-6-2-7-15-24)25-16-8-3-9-17-25/h1-17,26H,18-22H2/b13-10-

16699-20-0 Relevant articles

Iron-catalyzed synthesis of cinnarizine

Shakhmaev,Sunagatullina, A. Sh.,Zorin

, p. 95 - 97 (2015)

Cinnarizine was synthesized in a high yi...

Allyl coupling reaction method and application thereof

-

Paragraph 0304-0308, (2021/08/25)

The invention discloses a novel allyl co...

Oxidative Rearrangement of MIDA (N-Methyliminodiacetic Acid) Boronates: Mechanistic Insights and Synthetic Applications

Kaldas, Sherif J.,Tien, Chieh-Hung,Gomes, Gabriel Dos Passos,Meyer, Stephanie,Sirvinskas, Martynas,Foy, Hayden,Dudding, Travis,Yudin, Andrei K.

supporting information, p. 324 - 328 (2021/01/26)

Herein we report that coordinative hemil...

Scalable preparation of stable and reusable silica supported palladium nanoparticles as catalysts for N-alkylation of amines with alcohols

Alshammari, Ahmad S.,Natte, Kishore,Kalevaru, Narayana V.,Bagabas, Abdulaziz,Jagadeesh, Rajenahally V.

, p. 141 - 149 (2020/01/06)

The development of nanoparticles-based h...

Palladium-Based Hydroamination Catalysts Employing Sterically Demanding 3-Iminophosphines: Branched Kinetic Products by Prevention of Allylamine Isomerization

Thakuri, Rajendr S.,Schmidt, Joseph A. R.

, p. 1917 - 1927 (2019/05/21)

A new allylpalladium triflate catalyst w...

16699-20-0 Process route

: 4393-06-0
1-Phenyl-2-propen-1-ol

: 841-77-0
diphenylmethylpiperazine

: 298-57-7,16699-20-0
cinnarizine

Conditions

Conditions	Yield
With Pd(xantphos)(MeCN)₂(OTf)₂; In isopropyl alcohol; at 20 ℃; for 12h; Inert atmosphere;	95%

: 104-54-1
3-Phenylpropenol

: 841-77-0
diphenylmethylpiperazine

: 298-57-7,16699-20-0
cinnarizine