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1H-Indol-5-ol, 4-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135531-89-4

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135531-89-4 Usage

Classification

Nitro compound

Derivative

Indole derivative

Usage

Synthesis of pharmaceuticals, agrochemicals, and organic compounds

Properties

Nitroaromatic and indole properties

Application

Building block for producing biologically active molecules

Potential

Research and development in medicinal and organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 135531-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,5,3 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135531-89:
(8*1)+(7*3)+(6*5)+(5*5)+(4*3)+(3*1)+(2*8)+(1*9)=124
124 % 10 = 4
So 135531-89-4 is a valid CAS Registry Number.

135531-89-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-4-nitroindole

1.2 Other means of identification

Product number -
Other names -

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:135531-89-4 SDS

135531-89-4Upstream product

135531-89-4Downstream Products

135531-89-4Relevant academic research and scientific papers

SIMPLE SYNTHESES OF 1,3,4,5-TETRAHYDROPYRROLOQUINOLINE AND 5-HYDROXY-4-NITROINDOLE (SYNTHETIC STUDY FOR INDOLES HAVING A NITROGEN CONTAINING FUNCTIONAL GROUP AT THE 4-POSITION)

Hamabuchi, Shin,Hamada, Hirokazu,Hironaka, Akiko,Somei, Masanori

, p. 443 - 448 (2007/10/02)

A simple four (or three) step synthesis method for 1,3,4,5-tetrahydropyrroloquinoline (6) from indole-3-carboxaldehyde (9) is developed.A single step preparation of 5-hydroxy-4-nitroindole (8) by the oxidation of 4-aminoindole (16) is also reported.

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