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324076-69-9

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324076-69-9 Usage

General Description

The chemical 1-(4-(trifluoromethyl)phenethyl)-6,7-dimethoxy-3,4-dihydroisoquinoline is a compound with a complex molecular structure. It consists of a phenethyl group with a trifluoromethyl substitution, as well as two methoxy groups attached to a dihydroisoquinoline ring system. 1-(4-(TRIFLUOROMETHYL)PHENETHYL)-6,7-DIMETHOXY-3,4-DIHYDROISOQUINOLINE may have potential pharmacological properties due to its structural features, and it could be used in medicinal chemistry research or drug development. Its precise biological activities and potential therapeutic applications would need to be determined through further study and experimentation.

Check Digit Verification of cas no

The CAS Registry Mumber 324076-69-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,4,0,7 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 324076-69:
(8*3)+(7*2)+(6*4)+(5*0)+(4*7)+(3*6)+(2*6)+(1*9)=129
129 % 10 = 9
So 324076-69-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H20F3NO2/c1-25-18-11-14-9-10-24-17(16(14)12-19(18)26-2)8-5-13-3-6-15(7-4-13)20(21,22)23/h3-4,6-7,11-12H,5,8-10H2,1-2H3

324076-69-9SDS

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 6,7-dimethoxy-1-[2-[4-(trifluoromethyl)phenyl]ethyl]-3,4-dihydroisoquinoline

1.2 Other means of identification

Product number -
Other names -

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:324076-69-9 SDS

324076-69-9Relevant articles and documents

METHOD FOR OBTAINING AN OPTICALLY PURE 1,2,3,4 TETRAHYDRO-ISOQUINOLINE DERIVATIVE

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Page/Page column 26, (2010/06/20)

The invention relates to a method for obtaining enantiomerically enriched 6,7-dimethoxy-1-[2-(4-trifluoromethyl-phenyl)-ethyl]-1,2,3,4-tetrahydro-isoquinoline from a mixture of (R)-6,7-dimethoxy-1-[2-(4-trifluoromethyl-phenyl)-ethyl]-1,2,3,4-tetrahydro-isoquinoline and (S)-6,7-dimethoxy-1-[2-(4-trifluoromethyl-phenyl)-ethyl]-1,2,3,4-tetrahydro-isoquinoline.

PROCESS FOR THE PREPARATION OF AN ENANTIOMERIC TRISUBSTITUTED 3,4-DIHYDRO-ISOQUINOLINE DERIVATIVE

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Page/Page column 10, (2010/12/29)

The present invention relates to a process for the preparation of the compound of formula (7) which process comprises the hydrogenation of the compound of formula (4) using bis[chloro-1,5-cyclooctadiene-iridium], (S)-i-dicyclohexylphosphino-2-[(S)-α-(dime

TRISUBSTITUTED 3,4-DIHYDRO-1H-ISOQUINOLIN COMPOUND, PROCESS FOR ITS PREPARATION, AND ITS USE

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Page/Page column 7; 19, (2009/08/14)

The present invention relates to the compound of formula (7*)acetate (see below), a process for its preparation, and its use.

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