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1-(3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)-2-hydroxy-5,5-dimethyl-2-(trifluoromethyl)-5,6-dihydropyrrolo[2,1-a]isoquinolin-3(2H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129762-57-8

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129762-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129762-57-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,7,6 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 129762-57:
(8*1)+(7*2)+(6*9)+(5*7)+(4*6)+(3*2)+(2*5)+(1*7)=158
158 % 10 = 8
So 129762-57-8 is a valid CAS Registry Number.

129762-57-8SDS

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 1-(3,3-dimethyl-4H-isoquinolin-1-yl)-2-hydroxy-5,5-dimethyl-2-(trifluoromethyl)-6H-pyrrolo[2,1-a]isoquinolin-3-one

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:129762-57-8 SDS

129762-57-8Downstream Products

129762-57-8Relevant academic research and scientific papers

REACTIONS OF POLYFLUOROCARBONYL COMPOUNDS WITH 1,3,3-TRIMETHYL-3,4-DIHYDROISOQUINOLINE AND ITS DERIVATIVES

Sviridov, V. D.,Chkanikov, N. D.,Galakhov, M. V.,Shklyaev, Yu. V.,Shklyaev, V. S.,et al.

, p. 1268 - 1272 (1990)

1,3,3-Trimethyl-3,4-dihydroisoquinolines, which exist in the imine form, undergo C-hydroxyalkylation upon reaction with hexafluoroacetone and esters of trifluoropyruvic acid at the C1-CH3 group at 20 deg C.The products with the ketoesters are converted upon heating to γ-lactams.Derivatives of 1,3,3-trimethyl-3,4-dihydroisoquinoline substituted at C1-CH3 group and existing in the enamine form, react with esters of trifluoropyruvic acid at 20 deg C to give exclusively γ-lactams and do not give reaction products with hexafluoroacetone.

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