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188220

5-Phenyl-1-pentanol

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

98%

동의어(들):

Benzenepentanol

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About This Item

Linear Formula:

C₆H₅(CH₂)₅OH

CAS Number:

10521-91-2

Molecular Weight:

164.24

Beilstein:

1935233

EC Number:

234-064-8

MDL number:

MFCD00002979

UNSPSC 코드:

12352100

PubChem Substance ID:

24851308

NACRES:

NA.22

추천 제품

Slide 1 of 1

1 of 1

Sigma-Aldrich

197688

3-(3,4-Dimethoxyphenyl)-1-propanol

Quality Level

200

분석

98%

형태

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

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일반 설명

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

애플리케이션

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

픽토그램

GHS05

신호어

Danger

유해 및 위험 성명서

H318

예방조치 성명서

P280 - P305 + P351 + P338

Hazard Classifications

Eye Dam. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

230.0 °F - closed cup

Flash Point (°C)

110 °C - closed cup

개인 보호 장비

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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문서 라이브러리 방문

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)

Preparation and properties of gelatin-immobilized beta-glucosidase from Pyrococcus furiosus.

Hidetaka Nagatomo et al.

Bioscience, biotechnology, and biochemistry, 69(1), 128-136 (2005-01-25)

Hyperthermostable beta-glucosidase from Pyrococcus furiosus was enclosed in gelatin gel by cross-linking with transglutaminase. Gelatin-immobilized beta-glucosidase was considerably more thermostable than the native enzyme. Lyophilized immobilisate was stored at 90 degrees C for 1 month without loss of activity. The

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