Welcome to LookChem.com Sign In|Join Free
  • or
1-[(3E)-3-(trimethylsilyl)pent-3-en-1-yl]-2,3,4,9-tetrahydro-1H-beta-carboline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83665-54-7

Post Buying Request

83665-54-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

83665-54-7 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 20 carbon (C) atoms, 31 hydrogen (H) atoms, and 1 nitrogen (N) atom.

Explanation

Beta-carboline is a heterocyclic compound with a core structure consisting of a pyrrolo[2,3-b]indole. The compound in question is a derivative of this family, meaning it has a similar core structure with additional functional groups or modifications.

Explanation

The compound contains a trimethylsilyl group (-SiMe3), which is an organosilicon group consisting of a silicon atom bonded to three methyl groups. This group can influence the compound's reactivity, stability, and lipophilicity.

Explanation

The compound exists in a tetrahydro form, meaning it has four hydrogen atoms added to the core structure. This can influence the compound's stability, reactivity, and pharmacological properties.

Explanation

Beta-carboline derivatives, including 1-[(3E)-3-(trimethylsilyl)pent-3-en-1-yl]-2,3,4,9-tetrahydro-1H-beta-carboline, have been found to possess a wide range of pharmacological properties. These include anti-inflammatory, antioxidant, and neuroprotective activities.

Explanation

Some beta-carboline derivatives have been studied for their potential as anticancer agents, suggesting that 1-[(3E)-3-(trimethylsilyl)pent-3-en-1-yl]-2,3,4,9-tetrahydro-1H-beta-carboline may also have similar properties.

Explanation

Beta-carbolines have been studied for their effects on the central nervous system, indicating that 1-[(3E)-3-(trimethylsilyl)pent-3-en-1-yl]-2,3,4,9-tetrahydro-1H-beta-carboline may have potential applications in the treatment of neurological disorders or conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 83665-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,6 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83665-54:
(7*8)+(6*3)+(5*6)+(4*6)+(3*5)+(2*5)+(1*4)=157
157 % 10 = 7
So 83665-54-7 is a valid CAS Registry Number.

83665-54-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-[(E)-5-(2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)pent-2-en-3-yl]silane

1.2 Other means of identification

Product number -
Other names (E)-2,3,4,9-tetrahydro-1-[3-(trimethylsilyl)-3-pentenyl]-1H-pyrido[3,4-b]indole

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:83665-54-7 SDS

83665-54-7Relevant academic research and scientific papers

Stereocontrolled Synthesis of Exocyclic Trisubstituted Double Bonds by Stereospecific Iminium Ion-Vinylsilane Cyclizations. A Short Synthetic Route to Indoloquinolizidine Alkaloids

Overman, Larry E.,Malone, Thomas C.

, p. 5297 - 5300 (2007/10/02)

The reaction of (Z)- and (E)-trisubstituted vinylsilanes 9 and 10 with paraformaldehyde and acid proceeded with >98percent retention of configuration to give indoloquinolizidines 13 and 3 in excellent yield.This is the first demonstration that iminium ion-vinylsilane cyclizations occur with complete retention of configuration with either vinylsilane stereoisomer.The simple indole alkaloid dl-deplancheine (3) was prepared in a stereocontrolled fashion in 26percent overall yield from commercially available 1-(trimethylsilyl)propyne.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 83665-54-7