268402
4-异丙基苯甲酸
≥96%
别名:
枯茗酸, 枯酸
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关于此项目
线性分子式:
(CH3)2CHC6H4CO2H
化学文摘社编号:
分子量:
164.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
208-642-5
MDL number:
Assay:
≥96%
产品名称
4-异丙基苯甲酸, ≥96%
InChI key
CKMXAIVXVKGGFM-UHFFFAOYSA-N
InChI
1S/C10H12O2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h3-7H,1-2H3,(H,11,12)
SMILES string
CC(C)c1ccc(cc1)C(O)=O
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
Quality Level
Application
用 4-异丙基苯甲酸合成了三种锡取代的三有机锡羧酸酯。用光谱学和热力学方法，从锡原子配位数的角度对产物进行了全面表征。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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
Angiolini L, et al.
Journal of Organometallic Chemistry, 691(9), 1965-1972 (2006)
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
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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