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268402

Sigma-Aldrich

4-Isopropylbenzoic acid

≥96%

Synonym(s):

Cumic acid, Cuminic acid

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About This Item

Linear Formula:
(CH3)2CHC6H4CO2H
CAS Number:
536-66-3
Molecular Weight:
164.20
EC Number:
208-642-5
MDL number:
MFCD00002564
UNSPSC Code:
12352100
PubChem Substance ID:
24856271
NACRES:
NA.22

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

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
Angiolini L, et al.
Journal of Organometallic Chemistry, 691(9), 1965-1972 (2006)
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 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
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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