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N-alpha-Boc-(S)-2,3-Diaminopropionic Acid CAS 73259-81-1

N-alpha-Boc-(S)-2,3-Diaminopropionic Acid CAS 73259-81-1

N-alpha-Boc-(S)-2,3-Diaminopropionic acid
CAS 73259-81-1
Purity: 98.0%Min | Appearance: White to off-white powder
Molecular Formula: C8H16N2O4 | MW: 204.22
Einecs:
Synonyms: 3-amino-N-(tert-butoxycarbonyl)-L-alanine;L-Alanine, 3-amino-N-[(1,1-dimethylethoxy)carbonyl]-;Boc-Dapa-OH

Product Introduction

Dayang Chem (Hangzhou) Co., Ltd. is one of the leading manufacturers and suppliers of n-alpha-boc-(s)-2,3-diaminopropionic acid cas 73259-81-1 in China, specialized in providing high quality customized chemicals. Welcome to wholesale bulk n-alpha-boc-(s)-2,3-diaminopropionic acid cas 73259-81-1 made in China here and get pricelist from our factory. Good service and reasonable price are available.

 

Product Introduction:

 

1.     Specification

Appearance

White to off-white powder

Assay

98.0% Min

Melting Range

209~210

Loss on Drying

1.0% Max

 

The latest specifications and COA will be sent upon request.

 

2.     Packaging & shipping

Packaging

Bulk Packaging: 10kg ,25kg bag or drum or custom packaging upon request

Transport Classification

Not regulated as a dangerous good

Lead Time

in stock

Shipping Methods

DHL, FedEx, air freight or sea freight

f-N-alpha-Boc-S-23-Diaminopropionic acid

s-N-alpha-Boc-S-23-Diaminopropionic acid

 

3.     Applications

Boc-L-Dap-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

 

4.     Spectrum

t-73259-81-1-N-alpha-Boc-S-23-Diaminopropionic acid

 

 

5.     Related Articles

1. Glucosamine-6-phosphate synthase from Escherichia coli: determination of the mechanism of inactivation by N3-fumaroyl-L-2,3-diaminopropionic derivatives.Biochemistry   29 , 3668, (1990)
2. Antimicrobial properties of N3-(iodoacetyl)-L-2,3-diaminopropanoic acid-peptide conjugates.J. Med. Chem.   33 , 2755, (1990)
3. Minimum requirements for inhibition of smooth-muscle myosin light-chain kinase by synthetic peptides.Biochem. J.   257 , 73, (1989)

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