268402
4-Isopropylbenzoic acid
≥96%
Synonym(s):
Cumic acid, Cuminic acid
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About This Item
Linear Formula:
(CH3)2CHC6H4CO2H
CAS Number:
Molecular Weight:
164.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
≥96%
mp
117-120 °C (lit.)
solubility
alcohol: soluble(lit.)
diethyl ether: soluble(lit.)
sulfuric acid: soluble(lit.)
water: slightly soluble(lit.)
functional group
carboxylic acid
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
Related Categories
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 Code
11 - 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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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
Young J Choi et al.
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PmxaF is a strong methanol-inducible promoter in Methylobacterium extorquens. When this promoter is cloned in expression vectors and used to drive heterologous gene expression, methanol inducibility is either greatly reduced or entirely lost. In order to bestow inducibility upon the
L G Puskás et al.
DNA sequence : the journal of DNA sequencing and mapping, 11(1-2), 9-20 (2000-07-21)
Rhodopseudomonas palustris utilizes p-cumate as a carbon source both under anaerobic light and aerobic dark conditions. A gene cluster was isolated whose sequence showed high homology to genes which have been implicated the degradation of p-cumate in Pseudomonas pitida. Seven
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
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