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1-Phenylcyclobutanecarboxamide, a chemical compound with the molecular formula C11H13NO, is a derivative of cyclobutanecarboxamide featuring a phenyl group attached to the carbon atom. 1-PhenylcyclobutanecarboxaMide holds potential in medicinal chemistry due to its unique structure and reactivity, and has been studied for its potential as an analgesic and anti-inflammatory agent. As a relatively new compound, further research is necessary to fully explore its properties and applications.

17380-65-3

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17380-65-3 Usage

Uses

Used in Pharmaceutical Industry:
1-Phenylcyclobutanecarboxamide is used as a potential analgesic and anti-inflammatory agent for its potential to alleviate pain and reduce inflammation. Its unique structure and reactivity may contribute to its effectiveness in these applications.
Used in Organic Synthesis:
1-Phenylcyclobutanecarboxamide is used as a reagent in organic synthesis, where its unique structure and reactivity can be leveraged to facilitate various chemical reactions and the production of other compounds. Its potential in this area is still under investigation, with further research needed to understand its full capabilities and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 17380-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,8 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17380-65:
(7*1)+(6*7)+(5*3)+(4*8)+(3*0)+(2*6)+(1*5)=113
113 % 10 = 3
So 17380-65-3 is a valid CAS Registry Number.

17380-65-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Phenylcyclobutanecarboxamide

1.2 Other means of identification

Product number -
Other names 1-Phenylcyclobutylamin

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:17380-65-3 SDS

17380-65-3Relevant academic research and scientific papers

Hydration of Cyanohydrins by Highly Active Cationic Pt Catalysts: Mechanism and Scope

Li, Chengcheng,Chang, Xiao-Yong,Huo, Luqiong,Tan, Haibo,Xing, Xiangyou,Xu, Chen

, p. 8716 - 8726 (2021/07/26)

Cyanohydrins (α-hydroxy nitriles) are a special type of nitriles that readily decompose into hydrogen cyanide (HCN) and the corresponding carbonyl compounds. Hydration of cyanohydrins that are readily available through cyanation of aldehydes and ketones provides the most straightforward route to valuable α-hydroxyamides. However, due to low stability of cyanohydrins and deactivation of the catalysts by the released HCN, catalytic direct hydration of cyanohydrins still remains largely unsolved. As a general trend, cyanohydrins containing bulkier substituents, such as α,α-diaryl cyanohydrins, degrade more quickly and thus are more difficult to be hydrated. Here, we report development of cationic platinum catalysts that exhibit high reactivity for hydration of various cyanohydrins. Detailed mechanistic investigations for hydration of nitriles by (PμP)Pt(PR2OH)X(OTf) reveal a catalytic cycle involving the formation of a five-membered metallacyclic intermediate and subsequent hydrolysis via attacking on the phosphorus of the secondary phosphine oxide (PR2OH) ligand by H2O. We discovered that Pt catalyst A bearing the electron-rich, appropriately small-bite-angle bisphosphine ligand provides super reactivity for hydration of cyanohydrins. The hydration reactions catalyzed by A proceed at ambient temperatures and occur with a wide variety of cyanohydrins, including the most difficult α,α-diaryl cyanohydrins, with good turnover numbers.

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