Z-β-Ala-OH, 98%, Z-amino acids

Name: Z-β-Ala-OH, 98%, Z-amino acids | 2304-94-1
Brand: J&K Chemical
SKU: JK591365_5_G
Price: 10.0 USD
Availability: InStock

Cat. No JK591365_5_G

Vendor: J&K Chemical

Product Information

Product Name

Z-β-Ala-OH, 98%, Z-amino acids

Brand Name

J&K

Product Number

591365

CAS

2304-94-1

SDS Document

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Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

75313

IUPAC Name

3-(phenylmethoxycarbonylamino)propanoic acid

InChI Key

GEVGRLPYQJTKKS-UHFFFAOYSA-N

SMILES

C1=CC=C(C=C1)COC(=O)NCCC(=O)O

Safety Information

Storage Condition

Store at 2-8℃

References Data Source From Pubchem

3,3-Difluoroproline

Publication Name: Science of Synthesis

Publication Date: 2025

Interest of new alkylsulfonylhydrazide-type compound in the treatment of alcohol use disorders

Publication Name: Psychopharmacology

Publication Date: 2018-04-30

DOI: 10.1007/s00213-018-4917-5

Synthesis of actinomycin analogs: XXIV. Non-symmetric derivatives of actinocin containing benzo-18-crown-6 moiety and tertiary ammonium group

Publication Name: Russian Journal of General Chemistry

Publication Date: 2016-12

DOI: 10.1134/s1070363216120070

One-pot efficient synthesis of Nα-urethane-protected β- and γ-amino acids

Publication Name: Amino Acids

Publication Date: 2012-12-19

DOI: 10.1007/s00726-012-1443-3

Amphiphilic molecular gels from omega-aminoalkylated L-glutamic acid derivatives with unique chiroptical properties

Publication Name: Amino Acids

Publication Date: 2010-01-27

DOI: 10.1007/s00726-010-0480-z

Z-β-Ala-OH, 98%, Z-amino acids

Product Information

General Information

Safety Information

References Data Source From Pubchem

3,3-Difluoroproline

Interest of new alkylsulfonylhydrazide-type compound in the treatment of alcohol use disorders

Synthesis of actinomycin analogs: XXIV. Non-symmetric derivatives of actinocin containing benzo-18-crown-6 moiety and tertiary ammonium group

One-pot efficient synthesis of Nα-urethane-protected β- and γ-amino acids

Amphiphilic molecular gels from omega-aminoalkylated L-glutamic acid derivatives with unique chiroptical properties