4-Methoxycinnamic acid, predominantly trans 99%

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Related Categories	Aloe Vera, Building Blocks, C10, Carbonyl Compounds, Carboxylic Acids, Chemical Synthesis, Curcuma longa (Turmeric), Liquid Crystals, Materials Science, Nematic, Nutrition Research, Organic Building Blocks, Organic and Printed Electronics, Phytochemicals by Plant (Food/Spice/Herb) More...
assay	99%
mp	170-173 °C(lit.)
transition temp	crystalline phase to nematic phase 173.5 °C
	nematic phase to isotropic phase 190 °C

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25, 100 g in poly bottle

5 g in glass bottle

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Related Papers

Structure-activity relationships of 1'S-1'-acetoxychavicol acetate for inhibitory effect on NO production in lipopolysaccharide-activated mouse peritoneal macrophages. Hisashi Matsuda et al Bioorg. Med. Chem. Lett. 15, 1949-53, (2005)

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Certificate of Analysis

FT-IR Condensed Phase

FT-IR Raman

Safety Information

Symbol	GHS07
Signal word	Warning
Hazard statements	H315-H319-H335
Precautionary statements	P261-P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes (Europe)	Xi
Risk Statements (Europe)	36/37/38
Safety Statements (Europe)	26
WGK Germany	3
RTECS	UD3391300

Technical information & documentation associated with this product is available in the Safety & Documentation tab.

Papers

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Structure-activity relationships of 1'S-1'-acetoxychavicol acetate for inhibitory effect on NO production in lipopolysaccharide-activated mouse peritoneal macrophages. Hisashi Matsuda et al Bioorg. Med. Chem. Lett. 15, 1949-53, (2005)

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Synthesis and biological evaluation of helicid analogues as mushroom tyrosinase inhibitors. Wei Yi et al Bioorg. Med. Chem. Lett. 18, 6490-3, (2008)

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1-(1-Arylethylidene)thiosemicarbazide derivatives: a new class of tyrosinase inhibitors. Jinbing Liu et al Bioorg. Med. Chem. 16, 1096-102, (2008)

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A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds. Jinbing Liu et al Eur. J. Med. Chem. 44, 1773-8, (2009)

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Inhibitory effects of 5-benzylidene barbiturate derivatives on mushroom tyrosinase and their antibacterial activities. Qin Yan et al Eur. J. Med. Chem. 44, 4235-43, (2009)

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Synthesis and biological evaluation of novel 4-hydroxybenzaldehyde derivatives as tyrosinase inhibitors. Wei Yi et al Eur. J. Med. Chem. 45, 639-46, (2010)

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Synthesis and structure-activity relationships of phenylpropanoid amides of serotonin on tyrosinase inhibition. Toshiyuki Takahashi et al Bioorg. Med. Chem. Lett. 21, 1983-6, (2011)

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Evaluation of dihydropyrimidin-(2H)-one analogues and rhodanine derivatives as tyrosinase inhibitors. Jinbing Liu et al Bioorg. Med. Chem. Lett. 21, 2376-9, (2011)

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Structure-activity relationships of trans-substituted-propenoic acid derivatives on the nicotinic acid receptor HCA2 (GPR109A). J P D van Veldhoven et al Bioorg. Med. Chem. Lett. 21, 2736-9, (2011)

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Beil. 10,298

FT-IR 1 (2), 180:C / FT-IR 2 (2), 2637:A / IR-Spectra (2), 834:B / IR-Spectra (3), 952:H / NMR-Reference 2 (2), 176:D / RegBook 1 (2), 1775:K / Structure Index 1, 283:A:6

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4-Methoxycinnamic acid, predominantly trans

99%

Properties

Description

Packaging

Price and Availability

Related Papers

Documents

Safety Information

Papers

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