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2H-Isoindole-1-carboxylic acid, 4,5,6,7-tetrahydro-3-(phenylethynyl)-, methyl ester is a complex organic compound with the chemical formula C18H17NO2. It is a derivative of isoindole, a heterocyclic aromatic organic compound, and features a phenylethynyl group attached to the 3-position of the tetrahydroisoindole ring. The compound is characterized by its unique molecular structure, which includes a methyl ester group, indicating the presence of a carbonyl group bonded to an oxygen atom and a methyl group. This chemical is primarily used in the synthesis of various pharmaceuticals and other organic compounds due to its versatile structure and reactivity.

145100-03-4

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145100-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145100-03-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,1,0 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 145100-03:
(8*1)+(7*4)+(6*5)+(5*1)+(4*0)+(3*0)+(2*0)+(1*3)=74
74 % 10 = 4
So 145100-03-4 is a valid CAS Registry Number.

145100-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-carbomethoxy-3-(2'-phenylethynyl)-4,5,6,7-tetrahydro-2H-isoindole

1.2 Other means of identification

Product number -
Other names 3-Phenylethynyl-4,5,6,7-tetrahydro-2H-isoindole-1-carboxylic acid methyl ester

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:145100-03-4 SDS

145100-03-4Downstream Products

145100-03-4Relevant academic research and scientific papers

Dihydropyrromethenones by Pd(0)-Mediated Coupling of Iodopyrroles and Acetylenic Amides. Synthesis of the A,B-Ring Segment of Phytochrome

Jacobi, Peter A.,Guo, Jiasheng,Rajeswari,Zheng, Wanjun

, p. 2907 - 2916 (2007/10/03)

Dihydropyrromethenone derivative 32b, which constitutes the A,B-ring segment of phytochrome (6), has been prepared in enantiomerically pure form beginning with acetylenic amide 47b and iodopyrrole 27. The key steps involved the TBAF-catalyzed 5-exo-dig cyclization of the acetylenic pyrrole 48b, followed by thia-Mitsunobu inversion of the resulting alcohol derivative 31b.

Tetrapyrroles. IV. A highly efficient synthesis of homochiral dihydropyrromethenones via Pd○ mediated coupling of iodopyrroles and acetylenic amides

Jacobi, Peter A.,Rajeswari

, p. 6235 - 6238 (2007/10/02)

Homochiral dihydropyrromethenones of type 20 have been synthesized in a highly efficient manner by Pd○ mediated coupling of iodopyrrole 14 with acetylenic amides 18, followed by F- catalyzed 5-exo-dig cyclization. In analogous fashion, phytochr

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