3-(5-METHYL-FURAN-2-YL)-PROPIONALDEHYDE

Names

[ Name ]:
3-(5-METHYL-FURAN-2-YL)-PROPIONALDEHYDE

[Synonym ]:
N-cyclohexylcyclohexanamine,(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-6-(phenylmethoxycarbonylamino)hexanoic acid
MFCD00066511
Nalpha-BOC-Nepsilon-CBZ-L-Lysine DCHA
EINECS 241-018-0

Biological Activity

[Description]:

Boc-Lys(Z)-OH (DCHA) is a involves in synthesis thymosin β4, βg and β6 fragments, and increases E-rosette forming capacity in Lupus Nephritis model. Boc-Lys(Z)-OH (DCHA) involves in synthesis Boc-Lyz-OCH3 and acts as a reagent of peptidyl thrombin inhibitors production[1][2][3].

[Related Catalog]:

Signaling Pathways >> Others >> Others

Research Areas >> Inflammation/Immunology

[References]

[1]. Abiko, et al. Synthesis of six common amino acid sequence fragments of thymosins beta 4, beta 8 and beta 9 and determination of their effects on the low E-rosette forming cells of lupus nephritis patients. Chemical & pharmaceutical bulletin, 1984.

[2]. Cal PM, et al. Iminoboronates: a new strategy for reversible protein modification. J Am Chem Soc. 2012 Jun 20;134(24):10299-305.

[3]. Van Boeckel, et al. Preparation of peptidyl thrombin inhibitors: World Intellectual Property Organization, WO9807308. 1998-02-26.

Chemical & Physical Properties

[ Boiling Point ]:
587ºC at 760 mmHg

[ Melting Point ]:
114-116ºC

[ Molecular Formula ]:
C₃₁H₅₁N₃O₆

[ Molecular Weight ]:
561.75300

[ Flash Point ]:
308.8ºC

[ Exact Mass ]:
561.37800

[ PSA ]:
125.99000

[ LogP ]:
7.47510

[ Vapour Pressure ]:
1.26E-14mmHg at 25°C

[ Storage condition ]:
-20°C

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29224985

Precursor & DownStream

Precursor

DownStream

Related Compounds

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