Welcome to LookChem.com Sign In|Join Free

CAS

  • or

159388-68-8

Post Buying Request

159388-68-8 Suppliers

Recommended suppliersmore

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

159388-68-8 Usage

Molecular structure

A 5-hydroxyindole ring with a 1-methylethyl group attached at the 6th position

Classification

Indole class of organic compounds

Synthesis use

Commonly used in the synthesis of various pharmaceuticals

Building block

Serves as a building block in organic chemistry

Pharmacological activities

Has potential as an enzyme inhibitor and has anti-inflammatory properties

Potential use

May be used in the treatment of certain diseases and disorders

Check Digit Verification of cas no

The CAS Registry Mumber 159388-68-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,3,8 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 159388-68:
(8*1)+(7*5)+(6*9)+(5*3)+(4*8)+(3*8)+(2*6)+(1*8)=188
188 % 10 = 8
So 159388-68-8 is a valid CAS Registry Number.

159388-68-8SDS

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 5-hydroxy-6-(1-methylethyl)indole

1.2 Other means of identification

Product number -
Other names 6-Isopropyl-1H-indol-5-ol

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:159388-68-8 SDS

159388-68-8Downstream Products

159388-68-8Relevant articles and documents

Synthesis and pharmacological evaluation of new indole derivatives structurally related to thymoxamine

Leonardi,Riva,De Toma,Boi,Pennini,Sironi

, p. 551 - 559 (2007/10/02)

The synthesis and pharmacological evaluation of a series of pyrrolidine analogues of thymoxamine allowed access to the basic SAR for the aromatic substitution pattern. The results confirm the relevance of the simultaneous presence of the hydroxy and methyl groups on the benzene ring and prompted us to prepare the corresponding indole congener. The principle of the phenol-indol bioisosterism was confirmed by the results obtained. The introduction of the N-(2-methoxyphenyl)piperazine moiety instead of pyrrolidine changed the receptor affinity profile and introduced a good uroselectivity.

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 159388-68-8