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3-hydroxy-2-(3-methoxypropyl)-3-phenyl-2,3-dihydro-1H-isoindol-1-one is a complex organic compound with the molecular formula C18H19NO3. It is a derivative of isoindolone, a heterocyclic compound with a fused indole ring and a lactam group. This specific compound features a hydroxyl group at the 3-position, a 3-methoxypropyl group at the 2-position, and a phenyl group at the 3-position. The compound is characterized by its unique structure, which includes a dihydro-1H-isoindol-1-one core, indicating the presence of a partially saturated ring system. It is likely to have specific applications in the fields of pharmaceuticals, materials science, or as an intermediate in organic synthesis, given its structural complexity and the presence of functional groups that can participate in various chemical reactions.

3532-76-1

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3532-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3532-76-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,3 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3532-76:
(6*3)+(5*5)+(4*3)+(3*2)+(2*7)+(1*6)=81
81 % 10 = 1
So 3532-76-1 is a valid CAS Registry Number.

3532-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-2-(3-methoxypropyl)-3-phenylisoindol-1-one

1.2 Other means of identification

Product number -
Other names 3-Hydroxy-2-<3-methoxy-propyl>-3-phenyl-phthalimidin

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:3532-76-1 SDS

3532-76-1Downstream Products

3532-76-1Relevant academic research and scientific papers

Copper-catalysed synthesis of 3-hydroxyisoindolin-1-ones from benzylcyanide 2-iodobenzamides

Kavala, Veerababurao,Wang, Chen-Yu,Wang, Cheng-Chuan,Patil, Prakash Bhimrao,Fang, ChiaChi,Kuo, Chun-Wei,Yao, Ching-Fa

, p. 988 - 998 (2020/02/15)

An efficient one-pot two-step sequential reaction for the synthesis of biologically active 3-hydroxyisoindolin-1-one derivatives from 2-iodobenzamide derivatives and various substituted benzyl cyanides in the presence of CuCl and cesium carbonate in DMSO is reported. Furthermore, 3-hydroxyisoindolinone derivatives possessing bromo substituents were obtained from 2-iodobenzamide and 2-bromobenzyl cyanide substrates in two steps. Benzyl cyanide has been successfully used for the first time as a benzoyl synthon for the synthesis of 3-hydroxyisoindolin-1-ones. Interestingly, the mechanism of formation of 3-hydroxyisoindolin-1-ones is a novel pathway that involves carbon degradation followed by ring contraction.

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