N-Phenylacrylamide - CAS 2210-24-4

Catalog:	BB017376
Product Name:	N-Phenylacrylamide
CAS:	2210-24-4
Synonyms:	N-phenyl-2-propenamide; N-phenylprop-2-enamide

Technical Data

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Computed Properties

IUPAC Name:	N-phenylprop-2-enamide
Description:	N-Phenylacrylamide (CAS# 2210-24-4) is a useful research chemical.
Molecular Weight:	147.17
Molecular Formula:	C9H9NO
Canonical SMILES:	C=CC(=O)NC1=CC=CC=C1
InChI:	InChI=1S/C9H9NO/c1-2-9(11)10-8-6-4-3-5-7-8/h2-7H,1H2,(H,10,11)
InChI Key:	BPCNEKWROYSOLT-UHFFFAOYSA-N
Boiling Point:	145-150 °C (Press: 3 Torr)
Melting Point:	103-106 °C (lit.)
Purity:	> 98.0 % (GC) (N)
Density:	1.097±0.06 g/cm³(Predicted)
Appearance:	White to almost white powder to crystal
MDL:	MFCD00080617
LogP:	1.88410

Publication Number	Title	Priority Date
CN-113321765-A	Double-liquid-phase acid liquid thickener and preparation method thereof	20210803
CN-113321765-B	Double-liquid-phase acid liquid thickener and preparation method thereof	20210803
CN-113321766-A	Multi-element association type fracturing fluid thickening agent and preparation method thereof	20210803
CN-113321766-B	Multi-element association type fracturing fluid thickening agent and preparation method thereof	20210803
CN-113292573-A	Indolizine chromogen ketone compound with anti-tumor activity and preparation method and application thereof	20210609

PMID	Publication Date	Title	Journal
22705022	20120715	Synthesis, biological evaluation and molecular docking studies of 3-(1,3-diphenyl-1H-pyrazol-4-yl)-N-phenylacrylamide derivatives as inhibitors of HDAC activity	Bioorganic & medicinal chemistry
22224594	20120209	Discovery and structure-activity relationship of potent and selective covalent inhibitors of transglutaminase 2 for Huntington's disease	Journal of medicinal chemistry
22196975	20120201	A comparative assessment of α-lipoic acid N-phenylamides as non-steroidal androgen receptor antagonists both on and off gold nanoparticles	Bioorganic chemistry
22294093	20120131	Competing pathways control host resistance to virus via tRNA modification and programmed ribosomal frameshifting	Molecular systems biology
21469720	20110505	Effects of dynamical couplings in IR spectra of the hydrogen bond in N-phenylacrylamide crystals	The journal of physical chemistry. A

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Related Functional Groups

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[1018141-88-2]
1-(2-Cyanoethyl)-3-methyl-6-phenyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid
[1035840-45-9]
1-(5-Methoxy-1,3-benzoxazol-2-yl)piperidine-3-carboxylic acid
[1431966-64-1]
1-{2-[(3-Methoxypropyl)amino]-4-methyl-1,3-thiazol-5-yl}ethanone hydrochloride

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GHS Hazard Statement:	H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
Precautionary Statement:	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word:	Warning

Complexity:	148
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	147.068413911
Formal Charge:	0
Heavy Atom Count:	11
Hydrogen Bond Acceptor Count:	1
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	147.068413911
Rotatable Bond Count:	2
Topological Polar Surface Area:	29.1 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	1.8