(S)-3-Amino-2-azepanone, 98%

Name: (S)-3-Amino-2-azepanone, 98% | 21568-87-6
Brand: J&K Chemical
SKU: JK434320_250_MG
Price: 13.0 USD
Availability: OutOfStock

Cat. No JK434320_250_MG

Vendor: J&K Chemical

Product Information

Product Name

(S)-3-Amino-2-azepanone, 98%

Brand Name

J&K

Product Number

434320

CAS

21568-87-6

Molecular Formula

C6H12N2O

Molecular Weight

128.18

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

440599

IUPAC Name

(3S)-3-aminoazepan-2-one

InChI Key

BOWUOGIPSRVRSJ-YFKPBYRVSA-N

SMILES

C1CCNC(=O)C@H(C1)N

Safety Information

Storage Condition

Store at 2-8℃

References

Engineering nucleoside antibiotics toward the development of novel antimicrobial agents

Publication Name: The Journal of Antibiotics

Publication Date: 2019-09-09

DOI: 10.1038/s41429-019-0230-8

Refining and expanding nonribosomal peptide synthetase function and mechanism

Publication Name: Journal of Industrial Microbiology and Biotechnology

Publication Date: 2019-03-01

DOI: 10.1007/s10295-018-02130-w

Racemization of α-Amino Lactams

Publication Name: Science of Synthesis

Publication Date: 2015

Enantiospecific Total Synthesis of (−)-Bengamide E

Publication Name: Chemistry – An Asian Journal

Publication Date: 2012-12-03

DOI: 10.1002/asia.201200999

Development of Biocatalytic Processes in Japan and Germany: From Research Synergies to Industrial Applications

Publication Name: Chemistry – An Asian Journal

Publication Date: 2012-04-30

DOI: 10.1002/asia.201200105

(S)-3-Amino-2-azepanone, 98%

Product Information

General Information

Safety Information

References

Engineering nucleoside antibiotics toward the development of novel antimicrobial agents

Refining and expanding nonribosomal peptide synthetase function and mechanism

Racemization of α-Amino Lactams

Enantiospecific Total Synthesis of (−)-Bengamide E

Development of Biocatalytic Processes in Japan and Germany: From Research Synergies to Industrial Applications