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268402

Sigma-Aldrich

4-Isopropylbenzoesäure

≥96%

Synonym(e):

Cuminsäure

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About This Item

Lineare Formel:
(CH3)2CHC6H4CO2H
CAS-Nummer:
536-66-3
Molekulargewicht:
164.20
EG-Nummer:
208-642-5
MDL-Nummer:
MFCD00002564
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24856271
NACRES:
NA.22

Assay

≥96%

mp (Schmelzpunkt)

117-120 °C (lit.)

Löslichkeit

alcohol: soluble(lit.)
diethyl ether: soluble(lit.)
sulfuric acid: soluble(lit.)
water: slightly soluble(lit.)

SMILES String

CC(C)c1ccc(cc1)C(O)=O

InChI

1S/C10H12O2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h3-7H,1-2H3,(H,11,12)

InChIKey

CKMXAIVXVKGGFM-UHFFFAOYSA-N

Verwandte Kategorien

Anwendung

4-Isopropylbenzoic acid (cuminic acid) was used in the synthesis of three new triorganotin carboxylates bearing methyl, butyl and phenyl substituents at tin, respectively. The products were fully characterized by spectroscopic and thermal techniques, with regard to the coordination number of tin atom, in solution and in the solid state.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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4-tert-Butylbenzoylchlorid 98%

Sigma-Aldrich

157120

4-tert-Butylbenzoylchlorid

Natriumsalicylat ReagentPlus®, ≥99.5% (titration)

Sigma-Aldrich

S3007

Natriumsalicylat

3,4-Dihydroxy-benzoesäure ≥97.0% (T)

Sigma-Aldrich

37580

3,4-Dihydroxy-benzoesäure

R W Eaton
Journal of bacteriology, 178(5), 1351-1362 (1996-03-01)
Pseudomonas putida F1 utilizes p-cumate (p-isopropylbenzoate) as a growth substrate by means of an eight-step catabolic pathway. A 35.75-kb DNA segment, within which the cmt operon encoding the catabolism of p-cumate is located, was cloned as four separate overlapping restriction
Bruno Gaillet et al.
Biotechnology and bioengineering, 106(2), 203-215 (2010-02-24)
Fast and efficient production of recombinant proteins for structural and functional studies is a crucial issue for research and for industry. To this end, we have developed an efficient system to generate in less than 2 months, starting from the
R W Eaton
Journal of bacteriology, 179(10), 3171-3180 (1997-05-01)
Pseudomonas putida F1 utilizes p-cymene (p-isopropyltoluene) by an 11-step pathway through p-cumate (p-isopropylbenzoate) to isobutyrate, pyruvate, and acetyl coenzyme A. The cym operon, encoding the conversion of p-cymene to p-cumate, is located just upstream of the cmt operon, which encodes
Young J Choi et al.
Applied and environmental microbiology, 76(15), 5058-5066 (2010-06-22)
A novel tightly regulated gene expression system was developed for Escherichia coli by applying the regulatory elements of the Pseudomonas putida F1 cym and cmt operons to control target gene expression at the transcriptional level by using p-isopropylbenzoate (cumate) as
Bruno Gaillet et al.
Biotechnology progress, 23(1), 200-209 (2007-02-03)
To facilitate and accelerate the production of eukaryotic proteins with correct post-translational modifications, we have developed a protein production system based on the transduction of Chinese hamster ovary (CHO) cells using adenovirus vectors (AdVs). We have engineered a CHO cell
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