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197416

Sigma-Aldrich

3-(4-Hydroxyphenyl)-1-propanol

99%

Synonym(s):

1-(4-Hydroxyphenyl)-3-propanol, 3-(4-Hydroxyphenyl)propanol, 3-(p-Hydroxyphenyl)-1-propanol, 3-(p-Hydroxyphenyl)propyl alcohol, 4-(3-Hydroxypropyl)phenol, 4-Hydroxybenzenepropanol, Dihydro-p-coumaryl alcohol

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About This Item

Linear Formula:
HOC6H4(CH2)3OH
CAS Number:
Molecular Weight:
152.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

solid

mp

51-54 °C (lit.)

functional group

hydroxyl

SMILES string

OCCCc1ccc(O)cc1

InChI

1S/C9H12O2/c10-7-1-2-8-3-5-9(11)6-4-8/h3-6,10-11H,1-2,7H2

InChI key

NJCVPQRHRKYSAZ-UHFFFAOYSA-N

Application

3-(4-Hydroxyphenyl)-1-propanol was used in the synthesis of (−)-centrolobine.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Yangxin Wang et al.
Frontiers in bioengineering and biotechnology, 8, 714-714 (2020-08-01)
In situ immobilization of enzyme into metal-organic frameworks (MOFs) is performed through a one-step and facile method. Candida antarctica lipase B (CalB) is directly embedded in zeolitic imidazolate framework (ZIF)-8 by simply mixing an aqueous solution of 2-methylimidazole and zinc
Two successive one-pot reactions leading to the expeditious synthesis of (−)-centrolobine.
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Beer is a fermented beverage with beneficial phenolic compounds and is widely consumed worldwide. The current study aimed to describe the content of three families of phenolic compounds with relevant biological activities: prenylated flavonoids (from hops), simple phenolic alcohols (from
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