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

Modify Date: 2024-01-22 17:31:20

3-(5-METHYL-FURAN-2-YL)-PROPIONALDEHYDE structure	Common Name	3-(5-METHYL-FURAN-2-YL)-PROPIONALDEHYDE
	CAS Number	16948-04-2	Molecular Weight	561.75300
	Density	N/A	Boiling Point	587ºC at 760 mmHg
	Molecular Formula	C₃₁H₅₁N₃O₆	Melting Point	114-116ºC
	MSDS	USA	Flash Point	308.8ºC

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

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].

Name	boc-lys(z)-oh dcha
Synonym	More Synonyms

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.

Description

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.

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

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