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5-Hydroxy-2,3,4,9-tetrahydrocarbazole is an organic compound characterized by its off-white solid appearance. It is a chemical intermediate that plays a significant role in the synthesis of various pharmaceutical compounds.

35618-96-3

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35618-96-3 Usage

Uses

Used in Pharmaceutical Industry:
5-Hydroxy-2,3,4,9-tetrahydrocarbazole is used as an intermediate for the preparation of Vindoline analogues and Carvedilol derivatives. These analogues and derivatives are essential in the development of medications for various therapeutic applications, including cardiovascular and neurological disorders.
As a chemical intermediate, 5-Hydroxy-2,3,4,9-tetrahydrocarbazole contributes to the synthesis of complex drug molecules, enhancing their efficacy and safety. Its role in the pharmaceutical industry is crucial for the development of novel treatments and the improvement of existing medications.

Check Digit Verification of cas no

The CAS Registry Mumber 35618-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,6,1 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 35618-96:
(7*3)+(6*5)+(5*6)+(4*1)+(3*8)+(2*9)+(1*6)=133
133 % 10 = 3
So 35618-96-3 is a valid CAS Registry Number.

35618-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Hydroxy-2,3,4,9-tetrahydrocarbazole

1.2 Other means of identification

Product number -
Other names 6,7,8,9-tetrahydro-5H-carbazol-4-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:35618-96-3 SDS

35618-96-3Upstream product

35618-96-3Downstream Products

35618-96-3Relevant academic research and scientific papers

HYDROXYLATION OF INDOLINES AND INDOLES BY HYDROGEN PEROXIDE IN SUPERACIDS

Berrier, Christian,Jacquesy, Jean-Claude,Jouannetaud, Marie-Paule,Renoux, Alain

, p. 4565 - 4568 (2007/10/02)

In SbF5-HF, indolines and indoles are hydroxylated on the aromatic ring, protonated hydrogen peroxide H3O2+ reacting on the protonated substrates.

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