N-phenethylformamide, 97%

Name: N-phenethylformamide, 97% | 23069-99-0
Brand: J&K Chemical
SKU: JK1735436_1_G
Price: 81.3 USD
Availability: InStock

Cat. No JK1735436_1_G

Vendor: J&K Chemical

Product Information

Product Name

N-phenethylformamide, 97%

Brand Name

J&K

Product Number

1735436

CAS

23069-99-0

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

140995

IUPAC Name

N-(2-phenylethyl)formamide

InChI Key

NOOOMJZHMKSKBF-UHFFFAOYSA-N

SMILES

C1=CC=C(C=C1)CCNC=O

Safety Information

Storage Condition

Freezer -20℃

References Data Source From Pubchem

Isolation, structure elucidation, total synthesis, and biosynthesis of dermazolium A, an antibacterial imidazolium metabolite of a vaginal bacterium Dermabacter vaginalis

Publication Name: Archives of Pharmacal Research

Publication Date: 2023-01

DOI: 10.1007/s12272-022-01424-z

Laetiporus sulphureus (Bull.) Murrill - FOMITOPSIDACEAE

Publication Name: Ethnobiology of Uzbekistan

Publication Date: 2023

DOI: 10.1007/978-3-031-23031-8_115

A Practical Approach for the Transamidation of N,N-Dimethyl Amides with Primary Amines Promoted by Sodium tert-Butoxide under Solvent-Free Conditions

Publication Name: Synthesis

Publication Date: 2020-09-08

DOI: 10.1055/s-0040-1705892

Hydroperoxide-Mediated Decarboxylative Acylation of Amines with α-Keto Acids

Publication Name: Synfacts

Publication Date: 2020-02-18

DOI: 10.1055/s-0039-1691670

Formylation of Amines with CO2 by Using a Polymeric N-Heterocyclic Carbene

Publication Name: Synfacts

Publication Date: 2019-01-18

DOI: 10.1055/s-0037-1611171

N-phenethylformamide, 97%

Product Information

General Information

Safety Information

References Data Source From Pubchem

Isolation, structure elucidation, total synthesis, and biosynthesis of dermazolium A, an antibacterial imidazolium metabolite of a vaginal bacterium Dermabacter vaginalis

Laetiporus sulphureus (Bull.) Murrill - FOMITOPSIDACEAE

A Practical Approach for the Transamidation of N,N-Dimethyl Amides with Primary Amines Promoted by Sodium tert-Butoxide under Solvent-Free Conditions

Hydroperoxide-Mediated Decarboxylative Acylation of Amines with α-Keto Acids

Formylation of Amines with CO2 by Using a Polymeric N-Heterocyclic Carbene