Welcome to LookChem.com Sign In|Join Free

CAS

  • or
1H-Indol-3-ol, 5-bromo-4-chloro-, also known as 5-bromo-4-chloroindole, is a chemical compound with the molecular formula C8H5BrClNO. It is a derivative of indole, a heterocyclic aromatic organic compound. 1H-Indol-3-ol, 5-bromo-4-chlorofeatures both bromine and chlorine atoms, as well as a hydroxyl group attached to the indole ring. Its unique combination of functional groups makes it a valuable building block in organic synthesis and pharmaceutical research, due to its potential for creating novel chemical structures with biological activity.

117887-41-9 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 117887-41-9 Structure
  • Basic information

    1. Product Name: 1H-Indol-3-ol, 5-bromo-4-chloro-
    2. Synonyms: 1H-Indol-3-ol, 5-bromo-4-chloro-;1H-Indol-3-ol,5-broMo-4-chloro-,N-Boc;5-bromo-4-chloro-1H-Indol-3-ol
    3. CAS NO:117887-41-9
    4. Molecular Formula: C8H5BrClNO
    5. Molecular Weight: 246.4884
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 117887-41-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 437.863 °C at 760 mmHg
    3. Flash Point: 218.612 °C
    4. Appearance: /
    5. Density: 1.919 g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.763
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1H-Indol-3-ol, 5-bromo-4-chloro-(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1H-Indol-3-ol, 5-bromo-4-chloro-(117887-41-9)
    12. EPA Substance Registry System: 1H-Indol-3-ol, 5-bromo-4-chloro-(117887-41-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 117887-41-9(Hazardous Substances Data)

117887-41-9 Usage

Uses

Used in Organic Synthesis:
1H-Indol-3-ol, 5-bromo-4-chlorois used as a building block in organic synthesis for its ability to form new chemical structures with potential applications in various fields. Its presence of bromine and chlorine atoms, along with the hydroxyl group, allows for versatile chemical reactions and modifications, contributing to the development of new compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1H-Indol-3-ol, 5-bromo-4-chlorois utilized as a key intermediate in the development of new drugs. Its unique structure and functional groups enable the creation of molecules with specific biological activities, which can be further optimized for therapeutic applications. 1H-Indol-3-ol, 5-bromo-4-chloroplays a crucial role in the discovery and design of novel pharmaceutical agents with improved efficacy and selectivity.
Used in Material Science:
1H-Indol-3-ol, 5-bromo-4-chloroalso finds applications in material science, where its chemical properties can be exploited to develop new materials with specific properties. The presence of bromine and chlorine atoms, along with the indole ring, can influence the electronic, optical, and structural characteristics of the resulting materials, making them suitable for various applications such as sensors, catalysts, or advanced materials for electronics and energy storage.

Check Digit Verification of cas no

The CAS Registry Mumber 117887-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,8,8 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 117887-41:
(8*1)+(7*1)+(6*7)+(5*8)+(4*8)+(3*7)+(2*4)+(1*1)=159
159 % 10 = 9
So 117887-41-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H5BrClNO/c9-4-1-2-5-7(8(4)10)6(12)3-11-5/h1-3,11-12H

117887-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Indol-3-ol, 5-bromo-4-chloro-

1.2 Other means of identification

Product number -
Other names 5-bromo-4-chloro-3-hydroxyindole

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:117887-41-9 SDS

117887-41-9Relevant articles and documents

PH responsive Janus-like supramolecular fusion proteins for functional protein delivery

Kuan, Seah Ling,Ng, David Y. W.,Wu, Yuzhou,Foertsch, Christina,Barth, Holger,Doroshenko, Mikheil,Koynov, Kaloian,Meier, Christoph,Weil, Tanja

, p. 17254 - 17257 (2013)

A facile, noncovalent solid-phase immobilization platform is described to assemble Janus-like supramolecular fusion proteins that are responsive to external stimuli. A chemically postmodified transporter protein, DHSA, is fused with (imino)biotinylated cargo proteins via an avidin adaptor with a high degree of spatial control. Notably, the derived heterofusion proteins are able to cross cellular membranes, dissociate at acidic pH due to the iminobiotin linker and preserve the enzymatic activity of the cargo proteins β-galactosidase and the enzymatic subunit of Clostridium botulinum C2 toxin. The mix-and-match strategy described herein opens unique opportunities to access macromolecular architectures of high structural definition and biological activity, thus complementing protein ligation and recombinant protein expression techniques.

Detection of alkaline phosphatase using surface-enhanced raman spectroscopy

Ruan, Chuanmin,Wang, Wei,Gu, Baohua

, p. 3379 - 3384 (2006)

A new approach was developed to detect the activity of alkaline phosphatase (ALP) enzyme at ultralow concentrations using a surface-enhanced Raman scattering (SERS) technique. The approach is based on the use of gold nanoparticles as a SERS material whereas 5-bromo-4-chloro-3-indolyl phosphate (BCIP) is used as a substrate of ALP. The enzymatic hydrolysis of BCIP led to the formation of indigo dye derivatives, which were found to be highly SERS active. For the first time, we were able to detect ALP at a concentration of ~4 × 10-15 M or at single-molecule levels when ALP was incubated with BCIP for 1 h in the Tris-HCl buffer. The same technique also was successfully employed to detect surface-immobilized avidin, and a detection limit of 10 ng/mL was achieved. This new technique allows the detection of both free and labeled ALP as a Raman probe in enzyme immunoassays, immunoblotting, and DNA hybridization assays at ultralow concentrations.

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

What can I do for you?
Get Best Price

Get Best Price for 117887-41-9