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2(1H)-Isoquinolinecarboxaldehyde (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

208348-23-6

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208348-23-6 Usage

Appearance

Yellow to brown liquid

Odor

Sweet floral

Uses

Fragrance ingredient in perfumes and cosmetic products, precursor in the synthesis of pharmaceuticals and other organic compounds

Check Digit Verification of cas no

The CAS Registry Mumber 208348-23-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,3,4 and 8 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 208348-23:
(8*2)+(7*0)+(6*8)+(5*3)+(4*4)+(3*8)+(2*2)+(1*3)=126
126 % 10 = 6
So 208348-23-6 is a valid CAS Registry Number.

208348-23-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-isoquinoline-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-1H-ISOQUINOLINECARBOXALDEHYDE

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:208348-23-6 SDS

208348-23-6Downstream Products

208348-23-6Relevant academic research and scientific papers

Reductive formylation of isoquinoline derivatives with formamide and synthesis of 2-formyltetrahydroisoquinolines

Venkov, Atanas P.,Ivanov, Ilian I.

, p. 1433 - 1438 (1998)

Reductive formylation of isoquinoline derivatives as 3,4- dihydroisoquinolines 1, enamines and enamides of tetrahydroisoquinoline 2 and the reaction of 2-(2-acylphenyl)ethylamides 3 with formamide afforded the corresponding N-formyltetrahydroisoquinolines 4 and N- acyltetrahydroisoquinolines 5.

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