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1-phenyl-3,4-dihydroisoquinoline-2(1H)-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42063-87-6

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42063-87-6 Usage

Structure

Contains a phenyl group and a dihydroisoquinoline ring structure

Type

Carboxamide derivative

Potential uses

As an active pharmaceutical ingredient, particularly for cancer and neurological disorders

Biological activities

Antitumor and anti-inflammatory properties

Current status

Ongoing research into pharmacological properties and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 42063-87-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,6 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42063-87:
(7*4)+(6*2)+(5*0)+(4*6)+(3*3)+(2*8)+(1*7)=96
96 % 10 = 6
So 42063-87-6 is a valid CAS Registry Number.

42063-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-3,4-dihydro-1H-isoquinoline-2-carboxamide

1.2 Other means of identification

Product number -
Other names 1-phenyl-2-carbamoyl-1,2,3,4-tetrahydroisoquinoline

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:42063-87-6 SDS

42063-87-6Downstream Products

42063-87-6Relevant academic research and scientific papers

SELECTIVE REDUCTION of 2-CARBAMOYL-1-PHENYL-1,4-DIHYDROISOQUINOLIN-3(2H)-ONES

Zara-Kaczian, Erzsebet,Deak, Gyula,Toth, Gabor

, p. 2533 - 2555 (2007/10/02)

Treatment of 2-carbamoyl-1-phenyl-1,4-dihydroisoquinolin-3(2H)-ones (1) with lithium aluminium hydride or diborane resulted always in the reduction of the ring carbonyl group and, depending on the nature of the reducing agent and the structure of the starting compound 1,2,3,4-tetrahydro- (2), 1,2-dihydroisoquinoline derivatives (3) or 1,2,3,4-tetrahydroisoquinolin-3-ols (5) were obtained.

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