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3,6-Diacetyl-9-propyl-9H-carbazole is a complex organic compound belonging to the carbazole family, characterized by a tricyclic structure with a fused benzene ring and a pyrrole ring. It features two acetyl groups (-COCH3) attached at the 3rd and 6th positions, and a propyl group (-CH2CH2CH3) at the 9th position. 3,6-Diacetyl-9-propyl-9H-carbazole is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure. The presence of the acetyl and propyl groups significantly influences its chemical properties, such as reactivity and solubility, making it a valuable intermediate in organic synthesis.

1483-96-1

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1483-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1483-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,8 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1483-96:
(6*1)+(5*4)+(4*8)+(3*3)+(2*9)+(1*6)=91
91 % 10 = 1
So 1483-96-1 is a valid CAS Registry Number.

1483-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6-acetyl-9-propylcarbazol-3-yl)ethanone

1.2 Other means of identification

Product number -
Other names 3,6-Diacetyl-9-propyl-9H-carbazole

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:1483-96-1 SDS

1483-96-1Downstream Products

1483-96-1Relevant academic research and scientific papers

Design and synthesis of aryl-functionalized carbazole-based porous coordination cages

Rowland, Casey A.,Lorzing, Gregory R.,Bhattacharjee, Rameswar,Caratzoulas, Stavros,Yap, Glenn P. A.,Bloch, Eric D.

, p. 9352 - 9355 (2020)

A subset of coordination cages have garnered considerable recent attention for their potential permanent porosity in the solid state. Herein, we report a series of functionalized carbazole-based cages of the structure type M12(R-cdc)12 (M = Cr, Cu, Mo) where the functional groups include a range of aromatic substituents. Single-crystal X-ray structure determinations reveal a variety of intercage interactions in these materials, largely governed by pi-pi stacking. Density functional theory for a subset of these cages was used to confirm that the nature of the increased stability of aryl-functionalized cages is a result of inter-cage ligand interactions. This journal is

Synthesis and luminescence properties of nine novel carbazolyl diacylhydrazone Schiff-bases

Wu, Limin,Wu, Panliang,Guo, Dongcai,Fu, Wenqiang,Li, Dong,Luo, Tao

, p. 1 - 6 (2015)

Nine novel carbazolyl diacylhydrazone Schiff-bases were synthesized by alkylation, F-C acylation and condensation reactions starting from carbazole and hydrazide. The title Schiff-bases were characterized by 1H NMR, MS, IR and elemental analysis. The synthetic conditions were optimized, and the best yield of the title Schiff-bases was up to 92.3%. The relationships between the luminescence properties and the structures of the title Schiff-bases were studied. The results showed that the introduction of the Naphthalene-2-yloxy could form great plane conjugate structure to improve their luminescence properties.

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