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3-[1-(4-bromophenyl)-1H-pyrrol-2-yl]-2-naphthalen-2-ylprop-2-enenitrile is a complex organic compound with a molecular formula of C24H16BrN. It features a pyrrole ring fused to a naphthalene ring, with a bromophenyl group attached to the pyrrole. The molecule also contains a prop-2-enenitrile group, which is a three-carbon chain with a double bond and a nitrile group at the end. 3-[1-(4-bromophenyl)-1H-pyrrol-2-yl]-2-naphthalen-2-ylprop-2-enenitrile is likely to be used in the synthesis of pharmaceuticals or other organic compounds due to its unique structure and functional groups.

5501-13-3

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5501-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5501-13-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,0 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5501-13:
(6*5)+(5*5)+(4*0)+(3*1)+(2*1)+(1*3)=63
63 % 10 = 3
So 5501-13-3 is a valid CAS Registry Number.

5501-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[1-(4-bromophenyl)pyrrol-2-yl]-2-naphthalen-2-ylprop-2-enenitrile

1.2 Other means of identification

Product number -
Other names N-Benzyl-N-benzyloxycarbonyl-N'-benzyliden-hydrazin

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:5501-13-3 SDS

5501-13-3Downstream Products

5501-13-3Relevant academic research and scientific papers

An efficient solid-phase synthesis of 3-substituted and 3,3-disubstituted 1,2-dialkylpyrazolidine-3,5-diones

He, Rongjun,Lam, Yulin

scheme or table, p. 2182 - 2186 (2009/02/01)

An efficient and regioselective procedure for the synthesis of di-, tri- and fully-substituted pyrazolidine-3,5-diones on a solid-phase format is described. Microwave irradiation provided significant rate enhancement in this protocol. To demonstrate the v

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