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1035-19-4

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1035-19-4 Usage

Molecular Structure

The compound has a complex molecular structure that includes a sulfonyl group, a dihydroisoquinoline ring, and a carbonitrile functional group.

Organic Synthesis

It is commonly used in organic synthesis as a building block for constructing more complex molecules.

Potential Applications

The compound may have potential applications in medicinal chemistry and drug discovery.

Unique Structural Features

The compound has unique structural features that may contribute to its potential biological activities.

Further Research Needed

Additional research is required to fully explore the compound's potential uses and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1035-19-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,3 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1035-19:
(6*1)+(5*0)+(4*3)+(3*5)+(2*1)+(1*9)=44
44 % 10 = 4
So 1035-19-4 is a valid CAS Registry Number.

1035-19-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(benzenesulfonyl)-1H-isoquinoline-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-Benzolsulfonyl-1,2-dihydro-isochinolin-1-carbonitril

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:1035-19-4 SDS

1035-19-4Relevant articles and documents

Tetrahydrofolate Coenzyme Models: Synthesis of Tetrahydroimidazoisoquinolines and Tetrahydroimidazoquinolines

Jones, Raymond C. F.,Smallridge, Mark J.,Chapleo, Christopher B.

, p. 385 - 391 (2007/10/02)

The new dihydroimidazoles 3-methyl-1,5,6,10b-tetrahydroimidazoisoquinoline and 1-methyl-3,3a,4,5-tetrahydroimidazoquinoline are efficiently and conveniently prepared from isoquinoline and quinoline, via 1-aminomethyl-1,2,3,4-tetrahydroisoquinoline and 2-aminomethyl-1,2,3,4-tetrahydroquinoline, respectively.Deprotonation of the fused dihydroimidazoles at the methyl substituent leads to homologation via C-alkylation, C-acylation, or C-phosphonylation-condensation.The properties of the tetrahydroimidazoisoquinolines and tetrahydroimidazoquinolines towards reducing agents mirror those of monocyclic dihydroimidazoles, affording aminomethyl-isoquinolines and -quinolines, respectively.

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