N(Alpha)-Boc-L-2,3-Diaminopropionic Acid

Modify Date: 2024-01-02 18:11:14

N(Alpha)-Boc-L-2,3-Diaminopropionic Acid Structure
N(Alpha)-Boc-L-2,3-Diaminopropionic Acid structure
Common Name N(Alpha)-Boc-L-2,3-Diaminopropionic Acid
CAS Number 73259-81-1 Molecular Weight 204.22
Density 1.2±0.1 g/cm3 Boiling Point 364.4±37.0 °C at 760 mmHg
Molecular Formula C8H16N2O4 Melting Point 210ºC (dec.)
MSDS USA Flash Point 174.2±26.5 °C

 Use of N(Alpha)-Boc-L-2,3-Diaminopropionic Acid


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

 Names

Name N(Alpha)-Boc-L-2,3-Diaminopropionic Acid
Synonym More Synonyms

 N(Alpha)-Boc-L-2,3-Diaminopropionic Acid Biological Activity

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

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 364.4±37.0 °C at 760 mmHg
Melting Point 210ºC (dec.)
Molecular Formula C8H16N2O4
Molecular Weight 204.22
Flash Point 174.2±26.5 °C
Exact Mass 204.111008
PSA 101.65000
LogP 0.84
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.489

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases S24/25
RIDADR NONH for all modes of transport
WGK Germany 3

 Synthetic Route

~93%

N(Alpha)-Boc-L-2,3-Diaminopropionic Acid Structure

N(Alpha)-Boc-L-...

CAS#:73259-81-1

Literature: Kucharczyk, N.; Badet, B.; Goffic, F. Le Synthetic Communications, 1989 , vol. 19, # 9-10 p. 1603 - 1610

~16%

N(Alpha)-Boc-L-2,3-Diaminopropionic Acid Structure

N(Alpha)-Boc-L-...

CAS#:73259-81-1

Literature: Kucharczyk, N.; Badet, B.; Goffic, F. Le Synthetic Communications, 1989 , vol. 19, # 9-10 p. 1603 - 1610

 Precursor & DownStream

Precursor  1

DownStream  0

 Articles4

More Articles
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)

A mechanistic investigation of the inactivation of Escherichia coli glucosamine-6-phosphate synthase by N3-(4-methoxyfumaroyl)-L-2,3-diaminopropionate (FMDP) was undertaken. On the basis of the known ...

Antimicrobial properties of N3-(iodoacetyl)-L-2,3-diaminopropanoic acid-peptide conjugates.

J. Med. Chem. 33 , 2755, (1990)

Six peptide conjugates consisting of either norvaline, methionine, or lysine and N3-(iodoacetyl)-L-2,3-diaminopropanoic acid--a strong, irreversible inactivator of bacterial and fungal glucosamine-6-p...

Minimum requirements for inhibition of smooth-muscle myosin light-chain kinase by synthetic peptides.

Biochem. J. 257 , 73, (1989)

Although the amino acid residues that are important for peptide substrates of myosin light-chain kinase have been reported, those that are important for peptide inhibitors of this enzyme have not prev...

 Synonyms

L-Alanine, 3-amino-N-[(1,1-dimethylethoxy)carbonyl]-
(2S)-3-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
MFCD00236843
3-Amino-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-L-alanine
3-amino-N-(tert-butoxycarbonyl)-L-alanine
Boc-Dapa-OH
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