H-m-Fluoro-DL-Phe-OH

Name: H-m-Fluoro-DL-Phe-OH | 456-88-2
Brand: US-CATO
SKU: S57CPTD787924_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57CPTD787924_10_MG

Vendor: US-CATO

Product Information

Product Name

H-m-Fluoro-DL-Phe-OH

Brand Name

US-CATO

Product Number

CPTD787924

CAS

456-88-2

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

9976

IUPAC Name

2-amino-3-(3-fluorophenyl)propanoic acid

InChI Key

VWHRYODZTDMVSS-UHFFFAOYSA-N

SMILES

C1=CC(=CC(=C1)F)CC(C(=O)O)N

References Data Source From Pubchem

Approaches to α-Amino Acids Based on Deracemization and Stereoinversion

Publication Name: Science of Synthesis

Publication Date: 2019

Menaquinone-7 production from maize meal hydrolysate by Bacillus isolates with diphenylamine and analogue resistance

Publication Name: Journal of Zhejiang University. Science. B

Publication Date: 2017-06-21

DOI: 10.1631/jzus.b1600127

Rational and combinatorial approaches totttengineering styrene production by Saccharomycesttttcerevisiae

Publication Name: Microbial Cell Factories

Publication Date: 2014-08-21

DOI: 10.1186/s12934-014-0123-2

19F NMR Studies of a Desolvated Near-Native Protein Folding Intermediate

Publication Name: Biochemistry

Publication Date: 2013-08-16

DOI: 10.1021/bi4010057

Modulating substrate specificity of histone acetyltransferase with unnatural amino acids

Publication Name: Molecular BioSystems

Publication Date: 2011-08-31

DOI: 10.1039/c1mb05148b

H-m-Fluoro-DL-Phe-OH

Product Information

General Information

References Data Source From Pubchem

Approaches to α-Amino Acids Based on Deracemization and Stereoinversion

Menaquinone-7 production from maize meal hydrolysate by Bacillus isolates with diphenylamine and analogue resistance

Rational and combinatorial approaches totttengineering styrene production by Saccharomycesttttcerevisiae

19F NMR Studies of a Desolvated Near-Native Protein Folding Intermediate

Modulating substrate specificity of histone acetyltransferase with unnatural amino acids