CAS 16948-04-2|3-(5-METHYL-FURAN-2-YL)-PROPIONALDEHYDE

Introduction：Basic information about CAS 16948-04-2|3-(5-METHYL-FURAN-2-YL)-PROPIONALDEHYDE, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Table of Contents

1. Names
2. 3-(5-METHYL-FURAN-2-YL)-PROPIONALDEHYDE BiologicalActivity
3. Chemical & Physical Properties
4. Safety Information
5. Synonyms

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

Names

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

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

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 >>OthersResearch 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

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 >>OthersResearch 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
InChIKey	BQERJWRZLXZNIO-RSAXXLAASA-N
SMILES	C1CCC(NC2CCCCC2)CC1.CC(C)(C)OC(=O)NC(CCCCNC(=O)OCc1ccccc1)C(=O)O
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

Synonyms

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

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