361666
4-(Heptyloxy)benzoic acid
98%
Synonym(s):
4-n -Heptyloxybenzoic acid, p -(Heptyloxy)benzoic acid
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About This Item
Linear Formula:
CH3(CH2)6OC6H4CO2H
CAS Number:
Molecular Weight:
236.31
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
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Assay
98%
form
solid
mp
146 °C (lit.)
transition temp
crystalline phase to isotropic phase 146 °C
nematic phase to smectic phase <92 °C
nematic phase to isotropic phase 98 °C
SMILES string
CCCCCCCOc1ccc(cc1)C(O)=O
InChI
1S/C14H20O3/c1-2-3-4-5-6-11-17-13-9-7-12(8-10-13)14(15)16/h7-10H,2-6,11H2,1H3,(H,15,16)
InChI key
ZRVIYEJYXIDATJ-UHFFFAOYSA-N
Application
Intermediate for the synthesis of liquid crystals including chiral ferroelectric benzoates. Used in the preparation of medicinal compounds.
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Aldrichimica Acta, 23, 23-23 (1990)
Hyunshun Shin et al.
Bioorganic & medicinal chemistry, 15(7), 2617-2623 (2007-02-14)
The first committed step in lipid A biosynthesis is catalyzed by uridine diphosphate-(3-O-(R-3-hydroxymyristoyl))-N-acetylglucosamine deacetylase (LpxC), a zinc-dependent deacetylase, and inhibitors of LpxC may be useful in the development of antibacterial agents targeting a broad spectrum of Gram-negative bacteria. Here, we
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