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3-Methylisoquinolin-4-ol is an organic compound with the chemical formula C10H9NO. It is a derivative of isoquinoline, a heterocyclic aromatic organic compound with a benzene ring fused to a pyridine ring. This particular compound features a methyl group attached to the 3-position and a hydroxyl group at the 4-position of the isoquinoline structure. 3-Methylisoquinolin-4-ol is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its role as an intermediate in the production of certain alkaloids. It is also recognized for its potential biological activities, such as antioxidant properties, which are being studied for their implications in health and disease.

3336-53-6

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3336-53-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3336-53-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,3 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3336-53:
(6*3)+(5*3)+(4*3)+(3*6)+(2*5)+(1*3)=76
76 % 10 = 6
So 3336-53-6 is a valid CAS Registry Number.

3336-53-6SDS

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 4-hydroxy-3-methyl-isoquinoline

1.2 Other means of identification

Product number -
Other names 3-Methyl-4-hydroxyisochinolin

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:3336-53-6 SDS

3336-53-6Downstream Products

3336-53-6Relevant academic research and scientific papers

STUDIES ON SRN1 REACTIONS - 9 A NEW ACCESS TO THE ISOQUINOLINE RING SYSTEM

Beugelmans, Rene,Chastanet, Jacqueline,Roussi, Georges

, p. 311 - 314 (2007/10/02)

The SRN1 reaction between o-halogeno-benzylamines and enolates derived from a series of ketones and aldehydes affords 1, 2 dihydro-isoquinolines from which are obtained (i) the isoquinoline derivatives, either spontaneously or by treatment on Pd-C and (ii) the 1, 2, 3, 4 tetrahydro-isoquinoline derivatives after sodium borohydride reduction.

NOUVELLE SYNTHESE DU SQUELETTE DIHYDRO-1,2 ISOQUINOLEINE PAR REACTION DE SUBSTITUTION NUCLEOPHILE RADICALAIRE EN CHAINE (SRN1)

Beugelmans, R.,Chastanet, J.,Roussi, G

, p. 2313 - 2314 (2007/10/02)

The SRN1 reaction between ortho-iodo-benzylamine and ketone enolates affords the 1,2-dihydroisoquinoline ring system from which the 3-substituted isoquinolines or the 1,2,3,4-tetrahydroisoquinoline are obtained.

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