(E)-4-(3-Hydroxy-1-propen-1-yl)phenol - CAS 20649-40-5

Catalog:	BB016123
Product Name:	(E)-4-(3-Hydroxy-1-propen-1-yl)phenol
CAS:	20649-40-5
Synonyms:	4-[(E)-3-hydroxyprop-1-enyl]phenol; 4-[(E)-3-hydroxyprop-1-enyl]phenol

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	4-[(E)-3-hydroxyprop-1-enyl]phenol
Description:	(E)-4-(3-Hydroxy-1-propen-1-yl)phenol (CAS# 20649-40-5 ) is a useful research chemical.
Molecular Weight:	150.17
Molecular Formula:	C9H10O2
Canonical SMILES:	C1=CC(=CC=C1C=CCO)O
InChI:	InChI=1S/C9H10O2/c10-7-1-2-8-3-5-9(11)6-4-8/h1-6,10-11H,7H2/b2-1+
InChI Key:	PTNLHDGQWUGONS-OWOJBTEDSA-N
Melting Point:	213.5 °C
Appearance:	Solid
LogP:	1.39770

Publication Number	Title	Priority Date
CN-113416317-A	A method for separating C-type lignin and G/S-type lignin from seed coat of Euphorbiaceae plant	20210824
CN-113461680-A	4-hydroxycoumarin azaisatin derivative and preparation method and application thereof	20210629
CN-113265077-A	Bio-based TPU (thermoplastic polyurethane) film for express packaging and preparation method thereof	20210430
CN-113019435-A	Monoatomic palladium/molecular sieve catalyst, preparation thereof and application thereof in preparation of ketone by selective hydrogenation of biomass molecules	20210326
CN-113046864-A	Phenolic resin improved lignin carbon fiber and preparation method thereof	20210318

PMID	Publication Date	Title	Journal
32151596	20200425	p-Coumaric acid attenuates alcohol exposed hepatic injury through MAPKs, apoptosis and Nrf2 signaling in experimental models	Chemico-biological interactions
29879413	20180801	Antiproliferative effect of p-Coumaric acid targets UPR activation by downregulating Grp78 in colon cancer	Chemico-biological interactions
25824411	20150525	Antitumor activity of 4-O-(2″-O-acetyl-6″-O-p-coumaroyl-β-D-glucopyranosyl)-p-coumaric acid against lung cancers via mitochondrial-mediated apoptosis	Chemico-biological interactions
24001438	20131201	Cytotoxic and anti-inflammatory effects of onion peel extract on lipopolysaccharide stimulated human colon carcinoma cells	Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association
23810795	20130901	Sasa quelpaertensis Nakai extract and its constituent p-coumaric acid inhibit adipogenesis in 3T3-L1 cells through activation of the AMPK pathway	Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association

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GHS Hazard Statement:	H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
Precautionary Statement:	P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501
Signal Word:	Warning

Complexity:	124
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	1
Exact Mass:	150.068079557
Formal Charge:	0
Heavy Atom Count:	11
Hydrogen Bond Acceptor Count:	2
Hydrogen Bond Donor Count:	2
Isotope Atom Count:	0
Monoisotopic Mass:	150.068079557
Rotatable Bond Count:	2
Topological Polar Surface Area:	40.5 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	1.3