Key Documents

View All Documentation

188220

5-Phenyl-1-pentanol

Name: 5-Phenyl-1-pentanol
Brand: ALDRICH

98%

Synonym(s):

Benzenepentanol

Select a Size

Change View

About This Item

Linear Formula:

C₆H₅(CH₂)₅OH

CAS Number:

10521-91-2

Molecular Weight:

164.24

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24851308

EC Number:

234-064-8

Beilstein/REAXYS Number:

1935233

MDL number:

MFCD00002979

Assay:

98%

Form:

liquid

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

200

assay

98%

form

liquid

refractive index

n20/D 1.516 (lit.)

bp

155 °C/20 mmHg (lit.)

density

0.975 g/mL at 25 °C (lit.)

SMILES string

OCCCCCc1ccccc1

InChI

1S/C11H16O/c12-10-6-2-5-9-11-7-3-1-4-8-11/h1,3-4,7-8,12H,2,5-6,9-10H2

InChI key

DPZMVZIQRMVBBW-UHFFFAOYSA-N

Description

General description

5-Phenyl-1-pentanol undergoes oxidation in the presence of ceric ammonium nitrate to yield 2-benzyltetrahydrofuran.

Application

5-Phenyl-1-pentanol was used in the synthesis of:

methoxy and fluorine analogs of N-(piperidinyl)-1-(2,4-dichlorophenyl)-4-methyl-5-(4-pentylphenyl)-1H-pyrazole-3-carboxamide (O-1302)
2-[5-(4-iodophenyl)-pentyl]oxirane-2-carboxylic acid ethyl ester

hcodes

H318

pictograms

GHS05

signalword

Danger

pcodes

P280 - P305 + P351 + P338

Hazard Classifications

Eye Dam. 1

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Methoxy- and fluorine-substituted analogs of O-1302: synthesis and in vitro binding affinity for the CB1 cannabinoid receptor.

Shintaro Tobiishi et al.

Chemical & pharmaceutical bulletin, 55(8), 1213-1217 (2007-08-02)

Methoxy and fluorine analogs substituted on the terminal carbon of the pentyl chain of N-(piperidinyl)-1-(2,4-dichlorophenyl)-4-methyl-5-(4-pentylphenyl)-1H-pyrazole-3-carboxamide (O-1302) were synthesized in a multi-step process from 5-phenyl-1-pentanol, which was based on the 1,5-diarylpyrazole core template of N-(piperidinyl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide (SR141716) through condensation of the respective

Synthesis of [131I/123I]-2-[5-(4-iodophenyl)pentyl]oxirane-2- carboxylic acid ethyl ester.

H G Abbas et al.

International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 42(1), 7-11 (1991-01-01)

A method is described for the synthesis, purification and radiolabelling of [123I/131I]2-[5-(4-iodophenyl)-pentyl]oxirane-2-carboxylic acid ethyl ester. For the synthesis of this new agent, 5-phenylpentyl bromide (1), synthesized by reacting 5-phenyl-1-pentanol with sodium bromide under acidic conditions, was converted to diethyl 5-phenylpentylmalonate

Cyclic ether formation in oxidations of primary alcohols by cerium (IV). Reactions of 5-phenyl-1-pentanol, 4-phenyl-1-butanol, and 3-phenyl-1-propanol with ceric ammonium nitrate.

Doyle MP, et al.

The Journal of Organic Chemistry, 40(10), 1454-1456 (1975)

View All Related Papers

Global Trade Item Number

SKU	GTIN
188220-5G	04061837006357