230642
4-Heptylbenzoic acid
97%
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About This Item
Linear Formula:
CH3(CH2)6C6H4CO2H
CAS Number:
Molecular Weight:
220.31
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
253-894-1
Beilstein/REAXYS Number:
2047135
MDL number:
Assay:
97%
Form:
liquid crystal
InChI key
VSUKEWPHURLYTK-UHFFFAOYSA-N
InChI
1S/C14H20O2/c1-2-3-4-5-6-7-12-8-10-13(11-9-12)14(15)16/h8-11H,2-7H2,1H3,(H,15,16)
SMILES string
CCCCCCCc1ccc(cc1)C(O)=O
assay
97%
form
liquid crystal
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Jose Maria Moreno et al.
Materials (Basel, Switzerland), 12(12) (2019-06-20)
Different metalorganic lamellar hybrid materials based on associated nanoribbons were synthesized by the use of alkyl-benzyl monocarboxylate spacers, containing alkyl tails with variable lengths, which acted like structural growing inhibitors. These molecular agents were perpendicularly located and coordinated to aluminium
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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