Home Other Building Blocks 536-66-3
536-66-3,MFCD00002564
Catalog No.:AA00377M

536-66-3 | 4-Isopropylbenzoic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
95%
in stock  
$24.00   $17.00
- +
25g
95%
in stock  
$47.00   $33.00
- +
100g
95%
in stock  
$139.00   $97.00
- +
250g
95%
in stock  
$336.00   $235.00
- +
500g
95%
in stock  
$415.00   $290.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00377M
Chemical Name:
4-Isopropylbenzoic acid
CAS Number:
536-66-3
Molecular Formula:
C10H12O2
Molecular Weight:
164.2011
MDL Number:
MFCD00002564
SMILES:
CC(c1ccc(cc1)C(=O)O)C
Properties
Properties
 
BP:
271.8°C  
Form:
Solid  
MP:
117-120 °C(lit.)  
Refractive Index:
1.5198 (estimate)  
Solubility:
alcohol: soluble(lit.)  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
155  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
3.4  

Literature

Title: High-level recombinant protein production in CHO cells using lentiviral vectors and the cumate gene-switch.

Journal: Biotechnology and bioengineering 20100601

Title: Production of functionalized polyhydroxyalkanoates by genetically modified Methylobacterium extorquens strains.

Journal: Microbial cell factories 20100101

Title: A new classification system for bacterial Rieske non-heme iron aromatic ring-hydroxylating oxygenases.

Journal: BMC biochemistry 20080101

Title: The study of some polyphenolic compounds from Melissa officinalis L. (Lamiaceae).

Journal: Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi 20080101

Title: 3D-QSAR and molecular docking studies of benzaldehyde thiosemicarbazone, benzaldehyde, benzoic acid, and their derivatives as phenoloxidase inhibitors.

Journal: Bioorganic & medicinal chemistry 20070301

Title: Functional identification of p-cumate operons in the terpene-degrading Rhodococcus sp. strain T104.

Journal: FEMS microbiology letters 20070101

Title: High-level recombinant protein production in CHO cells using an adenoviral vector and the cumate gene-switch.

Journal: Biotechnology progress 20070101

Title: A study of chemical composition and antimicrobial activity of Bulgarian propolis.

Journal: Folia medica 20070101

Title: Identification and expression of the cym, cmt, and tod catabolic genes from Pseudomonas putida KL47: expression of the regulatory todST genes as a factor for catabolic adaptation.

Journal: Journal of microbiology (Seoul, Korea) 20060401

Title: Expansion of growth substrate range in Pseudomonas putida F1 by mutations in both cymR and todS, which recruit a ring-fission hydrolase CmtE and induce the tod catabolic operon, respectively.

Journal: Microbiology (Reading, England) 20030301

Title: Antifungal constituents of the stem bark of Bridelia retusa.

Journal: Phytochemistry 20030201

Title: Microsomal metabolism and enzyme kinetics of the terpene p-cymene in the common brushtail possum (Trichosurus vulpecula), koala (Phascolarctos cinereus) and rat.

Journal: Xenobiotica; the fate of foreign compounds in biological systems 20020501

Title: p-Cymene catabolic pathway in Pseudomonas putida F1: cloning and characterization of DNA encoding conversion of p-cymene to p-cumate.

Journal: Journal of bacteriology 19970501

Title: p-Cumate catabolic pathway in Pseudomonas putida Fl: cloning and characterization of DNA carrying the cmt operon.

Journal: Journal of bacteriology 19960301

Title: Jayasinghe L, et, al. Antifungal constituents of the stem bark of Bridelia retusa. Phytochemistry. 2003 Feb;62(4):637-41.

Title: Huang XH, et, al. Inhibition of the activity of mushroom tyrosinase by alkylbenzoic acids. Food Chemistry. 2006 Jan; 94(1): 1-6.

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Tags:536-66-3 Molecular Formula|536-66-3 MDL|536-66-3 SMILES|536-66-3 4-Isopropylbenzoic acid