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66040-34-4

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66040-34-4 Usage

Chemical compound

Yes

Physical state

Yellow-brown solid

Molecular weight

351.392 g/mol

Derivative of

Isoquinoline

Usage

Organic chemistry, synthetic and research purposes

Pharmacological and medicinal applications

Potentially studied

Chemical structure

Unique

Biological activities

Exhibits interesting properties

Drug development

Could potentially be utilized in the development of new drugs or pharmaceuticals

Check Digit Verification of cas no

The CAS Registry Mumber 66040-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,4 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66040-34:
(7*6)+(6*6)+(5*0)+(4*4)+(3*0)+(2*3)+(1*4)=104
104 % 10 = 4
So 66040-34-4 is a valid CAS Registry Number.

66040-34-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6,7-dimethoxy-1-phenyl-3,4-dihydro-1H-isoquinolin-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 2-acetyl-6,7-dimethoxy-1-phenyl-1,2,3,4-tetrahydro-isoquinoline

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:66040-34-4 SDS

66040-34-4Downstream Products

66040-34-4Relevant articles and documents

Synthesis and contractile activity of substituted 1,2,3,4- tetrahydroisoquinolines

Ivanov, Iliyan,Nikolova, Stoyanka,Aladjov, Dimo,Stefanova, Iliyana,Zagorchev, Plamen

, p. 7019 - 7042 (2011/11/05)

A series of different 1-monosubstituted and 1,1-disubstituted 1,2,3,4-tetrahydroisoquinolines was synthesized in high yields from different ketoamides. We have developed a convenient method for the synthesis of disubstituted derivatives by interaction of

Discovery of a novel and highly potent noncompetitive AMPA receptor antagonist

Gitto, Rosaria,Barreca, Maria Letizia,De Luca, Laura,De Sarro, Giovambattista,Ferreri, Guido,Quartarone, Silvana,Russo, Emilio,Constanti, Andrew,Chimirri, Alba

, p. 197 - 200 (2007/10/03)

N-Acetyl-1-aryl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline derivatives were designed and synthesized as potential noncompetitive AMPA receptor antagonists on the basis of molecular modeling studies. Sound-induced seizure testing showed that this class o

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