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Cyclopent-1-ene-1-carboxamide is a chemical compound with the molecular formula C6H9NO. It is a derivative of cyclopentane, an organic compound consisting of a five-membered ring of carbon and hydrogen atoms, with an amide group (-CONH2) attached to the first carbon atom. cyclopent-1-ene-1-carboxamide is characterized by its unique structure, which features a cyclopentane ring fused with an amide group, and is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals. Cyclopent-1-ene-1-carboxamide is a versatile building block in organic chemistry, and its properties can be further modified through functional group transformations to create a wide range of compounds with different applications.

5434-85-5

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5434-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5434-85-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5434-85:
(6*5)+(5*4)+(4*3)+(3*4)+(2*8)+(1*5)=95
95 % 10 = 5
So 5434-85-5 is a valid CAS Registry Number.

5434-85-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclopentene-1-carboxamide

1.2 Other means of identification

Product number -
Other names cyclopent-1-enecarboxamide

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:5434-85-5 SDS

5434-85-5Relevant academic research and scientific papers

Amino- and azidocarbonylation of iodoalkenes

Mikle, Gábor,Skoda-F?ldes, Rita,Kollár, László

, (2021/10/14)

Iodoalkenes, available from ketones via their hydrazones, underwent palladium-catalysed azidocarbonylation. Depending on the structure of the acyl azides, consecutive hydrolysis toward corresponding primary amides was observed. ‘Direct’ aminocarbonylation

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