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(1,3-dioxo-1,3,3a,4,7,7a-hexahydro-2H-isoindol-2-yl)acetic acid is a complex chemical compound belonging to the isoindole family. It features a dioxo group, an isoindolyl group, and an acetic acid group within its molecular structure. (1,3-dioxo-1,3,3a,4,7,7a-hexahydro-2H-isoindol-2-yl)acetic acid holds potential for use in the pharmaceutical industry, particularly as a building block for the synthesis of innovative drug molecules. The presence of the dioxo and isoindolyl groups indicates that it may possess unique chemical and biological properties, warranting further research and development. Careful handling and storage are necessary due to its potential reactivity and toxicity.

39059-06-8

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39059-06-8 Usage

Uses

Used in Pharmaceutical Industry:
(1,3-dioxo-1,3,3a,4,7,7a-hexahydro-2H-isoindol-2-yl)acetic acid is used as a building block for the synthesis of novel drug molecules due to its complex molecular structure and the presence of functional groups that may contribute to interesting chemical and biological properties. Its potential applications in drug development make it a target for further research and exploration.

Check Digit Verification of cas no

The CAS Registry Mumber 39059-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,5 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39059-06:
(7*3)+(6*9)+(5*0)+(4*5)+(3*9)+(2*0)+(1*6)=128
128 % 10 = 8
So 39059-06-8 is a valid CAS Registry Number.

39059-06-8SDS

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 2-(1,3-dioxo-3a,4,7,7a-tetrahydroisoindol-2-yl)acetic acid

1.2 Other means of identification

Product number -
Other names (1,3-Dioxo-1,3,3a,4,7,7a-hexahydro-isoindol-2-yl)-acetic acid

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:39059-06-8 SDS

39059-06-8Relevant academic research and scientific papers

Synthesis of Amides of Carboxylic Acids with an Imide and Alicyclic Fragments and a Study of Their Genotoxic Activity in the Allium Test

Firstova,Kofanov,Zakshevskaya,Kovaleva

, p. 204 - 213 (2019/07/02)

A method for the high-yield synthesis of several amides of carboxylic acids containing an imide, a cyclohexene, and a norbornene cycle as well as fragments of natural amino acids has been developed. The compounds synthesized have been tested for mutagenic activity on plant objects using the Allium test. It has been shown that the presence of a nitro group endows the compound with inhibitory property and the capacity to induce chromosomal rearrangements, whereas the presence of an aliphatic carbon chain, a methyl group, and a morpholine fragment, on the contrary, confers growth-regulating properties without inducing the mutagenic effect. The study has confirmed that the resulting biologically active compounds are of interest for practical implementation in agriculture.

ISOINDOLEDIONE DERIVATIVES AS ADRENERGIC RECEPTOR ANTAGONISTS

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Page/Page column 30, (2010/11/26)

Provided are isoindoledione derivatives, which can be used of treating a disease or disorder mediated through αla and/or α1(1 adrenergic receptors. Compounds disclosed herein can be used of treating benign prostatic hyperplasia (BPH) and related symptoms

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