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3998-04-7

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3998-04-7 Usage

General Description

9-Allylcarbazole is a chemical compound with the molecular formula C14H13N. It is a derivative of carbazole, containing both an allyl and a carbazole group. 9-ALLYLCARBAZOLE has applications in various fields, including organic synthesis, materials science, and pharmaceutical research. It can be used as a building block in the synthesis of organic compounds, as well as a monomer for the production of polymers. Additionally, 9-allylcarbazole has been investigated for its potential use in optoelectronic devices, such as organic light-emitting diodes (OLEDs), due to its favorable electronic and photophysical properties. In the pharmaceutical industry, it has been studied for its potential biological activities and therapeutic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 3998-04-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,9 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3998-04:
(6*3)+(5*9)+(4*9)+(3*8)+(2*0)+(1*4)=127
127 % 10 = 7
So 3998-04-7 is a valid CAS Registry Number.

3998-04-7SDS

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 9-prop-2-enylcarbazole

1.2 Other means of identification

Product number -
Other names 9-Allyl-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:3998-04-7 SDS

3998-04-7Relevant articles and documents

Design, synthesis and antifungal activity of carbazole derivatives

Zhu, Shi-Ping,Wang, Wen-Ya,Fang, Kun,Li, Zheng-Gang,Dong, Guo-Qiang,Miao, Zhen-Yuan,Yao, Jian-Zhong,Zhang, Wan-Nian,Sheng, Chun-Quan

, p. 229 - 233 (2014/02/14)

The incidence of invasive fungal infections is increasing rapidly. Clinically available antifungal agents suffer from limited efficacy and severe resistance. There is an urgent need to discover antifungal lead compounds with novel chemical scaffold. On the basis of our previously identified tetrahydrocarbazole antifungal leads, the structure-activity relationship was further explored by modifying the scaffold and the side chains. Several targeted compounds showed potent activity against Candida species. Particularly, compound 13i showed better antifungal activity than the lead compound, which can be used as a good starting point for further optimization.

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