(R)-2-Phenyl-1-propanol - CAS 19141-40-3

Catalog:	BB014809
Product Name:	(R)-2-Phenyl-1-propanol
CAS:	19141-40-3
Synonyms:	(2R)-2-phenyl-1-propanol; (2R)-2-phenylpropan-1-ol

Technical Data

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Computed Properties

IUPAC Name:	(2R)-2-phenylpropan-1-ol
Description:	(R)-2-Phenyl-1-propanol (CAS# 19141-40-3 ) is a useful research chemical.
Molecular Weight:	136.19
Molecular Formula:	C9H12O
Canonical SMILES:	CC(CO)C1=CC=CC=C1
InChI:	InChI=1S/C9H12O/c1-8(7-10)9-5-3-2-4-6-9/h2-6,8,10H,7H2,1H3/t8-/m0/s1
InChI Key:	RNDNSYIPLPAXAZ-QMMMGPOBSA-N
Boiling Point:	110-111 °C / 10 mmHg (lit.), 232.2 °C at 760 mmHg
Density:	0.975 g/cm³
MDL:	MFCD00145206
LogP:	1.78240

Publication Number	Title	Priority Date
JP-2021132557-A	Alcohol production method and enzyme-modified electrode	20200226
WO-2021071843-A1	Muscarinic acetylcholine m1 receptor antagonists	20191007
US-2021147400-A1	Method for producing (2s)-2-[(1h-pyrazol-1-yl)methyl]-1,3-oxazinane derivative	20170713
WO-2018116285-A1	Substituted morpholine derivatives as ror gamma modulators	20161223
US-10457669-B2	Benzolactam compounds as protein kinase inhibitors	20151021

PMID	Publication Date	Title	Journal
22055107	20120101	Characterization and further stabilization of a new anti-prelog specific alcohol dehydrogenase from Thermus thermophilus HB27 for asymmetric reduction of carbonyl compounds	Bioresource technology
17441121	20061218	Asymmetric resolution in ester reduction by NaBH4 at the interface of aqueous aggregates of amino acid, peptide, and chiral-counterion-based cationic surfactants	Chemistry, an Asian journal

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Complexity:	84.7
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	1
Defined Bond Stereocenter Count:	0
Exact Mass:	136.088815002
Formal Charge:	0
Heavy Atom Count:	10
Hydrogen Bond Acceptor Count:	1
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	136.088815002
Rotatable Bond Count:	2
Topological Polar Surface Area:	20.2
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	2.4