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Cyclohexanepropiolamide (8CI), also known as 1-cyclohexanepropanamide, is an organic compound with the chemical formula C9H17NO. It is a derivative of cyclohexane, with a propionamide group attached to the cyclohexane ring. Cyclohexanepropiolamide (8CI) is a colorless liquid with a molecular weight of 157.24 g/mol. Cyclohexanepropiolamide is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also known for its potential applications in the development of new materials and chemical processes. Due to its versatile structure, it has attracted interest in the field of organic chemistry and drug design.

4361-26-6

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4361-26-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4361-26-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4361-26:
(6*4)+(5*3)+(4*6)+(3*1)+(2*2)+(1*6)=76
76 % 10 = 6
So 4361-26-6 is a valid CAS Registry Number.

4361-26-6SDS

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 cyclohexyl-propiolic acid amide

1.2 Other means of identification

Product number -
Other names Cyclohexyl-propiolsaeure-amid

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:4361-26-6 SDS

4361-26-6Downstream Products

4361-26-6Relevant academic research and scientific papers

Catalytic, transition-metal-free semireduction of propiolamide derivatives: Scope and mechanistic investigation

Grams, R. Justin,Garcia, Christopher J.,Szwetkowski, Connor,Santos, Webster L.

, p. 7013 - 7018 (2020/09/12)

We report a transition-metal-free trans-selective semireduction of alkynes with pinacolborane and catalytic potassium tert-butoxide. A variety of 3-substituted primary and secondary propiolamides, including an analog of FK866, a potent nicotinamide mononucleotide adenyltransferase (NMNAT) inhibitor, are reduced to the corresponding (E)-3-substituted acrylamide derivatives in up to 99% yield with >99:1 E/Z selectivity. Mechanistic studies suggest that an activated Lewis acid-base complex transfers a hydride to the α-carbon followed by rapid protonation in a trans fashion.

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