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1H-Isoindole-1,3(2H)-dione, 2-(2-acetylphenyl)-4-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

143583-67-9

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143583-67-9 Usage

Physical form

Yellow to orange powder

Solubility

Insoluble in water, soluble in organic solvents

Uses

Intermediate in the synthesis of pharmaceutical compounds and dyes, preparation of organic semiconductors, building block in organic chemistry

Biological activity

Potential medicinal and therapeutic properties

Hazardous effects

Potential hazardous effects, handle with caution

Check Digit Verification of cas no

The CAS Registry Mumber 143583-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,5,8 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143583-67:
(8*1)+(7*4)+(6*3)+(5*5)+(4*8)+(3*3)+(2*6)+(1*7)=139
139 % 10 = 9
So 143583-67-9 is a valid CAS Registry Number.

143583-67-9SDS

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 2-(2-acetylphenyl)-4-nitroisoindole-1,3-dione

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:143583-67-9 SDS

143583-67-9Relevant academic research and scientific papers

Synthesis, spectroscopic studies, and x-ray crystal structure of N-heteryliminophosphoranes

Alkhathlan,Al-Jaradah,Al-Farhan,Mousa

, p. 373 - 388 (2004)

N-[2-(α-Bromoacetyl)phenyl]imides (prepared in two steps from 2-aminoacetophenone) gave, upon treatment with sodium azide, fused azidoquinolines via an intramolecular cyclization. Reaction of the above azides with phosphines gave N-heteryliminophosphoranes. The IR, 1H-, 13C-, and 31P-NMR and MS spectra of these compounds as well as the x-ray crystal structure of two of them is reported.

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