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

Modify Date: 2025-08-20 19:56:23

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.

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

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	Research Areas >> Others Signaling Pathways >> Others >> Others

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

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

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

Boc-L-Serine-be...

CAS#:98541-64-1

~93%

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

Boc-L-Serine-be...

CAS#:98541-64-1

~16%

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

CAS#:73259-81-1

N/A

CAS#:126330-78-7

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

Precursor 1
CAS#:98541-64-1 Boc-L-Serine-be...
DownStream 0

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...

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