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268402

Sigma-Aldrich

4-Isopropylbenzoic acid

≥96%

Sinónimos:

Cumic acid, Cuminic acid

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About This Item

Fórmula lineal:
(CH3)2CHC6H4CO2H
Número de CAS:
536-66-3
Peso molecular:
164.20
EC Number:
208-642-5
MDL number:
MFCD00002564
UNSPSC Code:
12352100
PubChem Substance ID:
24856271
NACRES:
NA.22

Quality Level

100

assay

≥96%

mp

117-120 °C (lit.)

solubility

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)

InChI key

CKMXAIVXVKGGFM-UHFFFAOYSA-N

Categorías relacionadas

Application

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.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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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, 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
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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