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6-chloro-2-nitrophenanthridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53364-98-0

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53364-98-0 Usage

Physical State

Yellow crystalline solid

Applications

Synthesis of pharmaceuticals and dyes
Potential biological activity
Investigated for antimicrobial properties
Cytotoxicity against cancer cells
Potential as an anticancer agent

Safety

Handle with care due to potential toxic or hazardous properties.

Check Digit Verification of cas no

The CAS Registry Mumber 53364-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,6 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53364-98:
(7*5)+(6*3)+(5*3)+(4*6)+(3*4)+(2*9)+(1*8)=130
130 % 10 = 0
So 53364-98-0 is a valid CAS Registry Number.

53364-98-0SDS

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 6-chloro-2-nitrophenanthridine

1.2 Other means of identification

Product number -
Other names 6-Chlor-2-nitro-phenanthridin

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:53364-98-0 SDS

53364-98-0Downstream Products

53364-98-0Relevant academic research and scientific papers

PYRROLOPHENANTHRIDINES IV. SYNTHESIS OF 3H-PYRROLO- AND 3H-PYRROLOPHENANTHRIDINES. REACTIVITY OF 3H-PYRROLOPHENANTHRIDINE

Baberkina, E. P.,Samoilova, M. E.,Buyanov, V. N.,Akhvlediani, R. N.,Levina, I. I.,et al.

, p. 961 - 968 (2007/10/02)

The nitration of 1- and 3-methylphenanthridines gave 1-methyl-2-nitro- and 3-methyl-4-nitrophenanthridines, which were converted by the Leimgruber method into 3H-pyrrolo- and 3H-pyrrolophenanthridines. 3H-Pyrrolophenanthridine was obtained by the Fischer reaction from 2-aminophenanthridine.The aminomethylation, formylation and amination of 3H-pyrrolophenanthridine were studied.

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