Home Other Building Blocks 4026-05-5
4026-05-5,MFCD00515124
Catalog No.:AA00CLCT

4026-05-5 | 3-(tert-Butyl)benzene-1,2-diol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
95%
2 weeks  
$141.00   $99.00
- +
250mg
95%
2 weeks  
$222.00   $155.00
- +
1g
95%
2 weeks  
$400.00   $280.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00CLCT
Chemical Name:
3-(tert-Butyl)benzene-1,2-diol
CAS Number:
4026-05-5
Molecular Formula:
C10H14O2
Molecular Weight:
166.2170
MDL Number:
MFCD00515124
SMILES:
Oc1cccc(c1O)C(C)(C)C
Properties
Computed Properties
 
Complexity:
148  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
2.9  

Literature

Title: Facial leucoderma following eczema: a new case induced by spectacle frames.

Journal: Contact dermatitis 20111001

Title: Radical chain reduction of alkylboron compounds with catechols.

Journal: Journal of the American Chemical Society 20110420

Title: Isolation and characterization of 4-tert-butylphenol-utilizing Sphingobium fuliginis strains from Phragmites australis rhizosphere sediment.

Journal: Applied and environmental microbiology 20101001

Title: Molecular structure and catechol oxidase activity of a new copper(I) complex with sterically crowded monodentate N-donor ligand.

Journal: Journal of inorganic biochemistry 20090301

Title: Anti-inflammatory effects of catechols in lipopolysaccharide-stimulated microglia cells: inhibition of microglial neurotoxicity.

Journal: European journal of pharmacology 20080624

Title: Neuronal effects of 4-t-Butylcatechol: a model for catechol-containing antioxidants.

Journal: Toxicology and applied pharmacology 20080415

Title: Enzymatic oxidation of tert-butylcatechol in the presence of sulfhydryl compounds: Application to the amperometric detection of penicillamine.

Journal: Talanta 20070227

Title: A green method for the electroorganic synthesis of new 1,3-Indandione derivatives.

Journal: Chemical & pharmaceutical bulletin 20061001

Title: The conformational state of polyphenol oxidase from field bean (Dolichos lablab) upon SDS and acid-pH activation.

Journal: The Biochemical journal 20060501

Title: Effect of AOT on enzymatic activity of the organic solvent resistant tyrosinase from Streptomyces sp. REN-21 in aqueous solutions and water-in-oil microemulsions.

Journal: Journal of colloid and interface science 20050415

Title: Inhibition of peroxidase-catalyzed oxidation of 3,3 ,5,5 -tetramethylbenzidine by aminophenols.

Journal: Biochemistry. Biokhimiia 20050301

Title: Purification and characterization of tyrosinase from gill tissue of Portabella mushrooms.

Journal: Phytochemistry 20040301

Title: Synthesis of 3-tert-butylcatechol by an engineered monooxygenase.

Journal: Biotechnology and bioengineering 20030305

Title: Optimizing the patch-test concentration of para-tertiary-butylcatechol: results of a prospective study with a dilution series.

Journal: Contact dermatitis 20030301

Title: Hysteresis and positive cooperativity of iceberg lettuce polyphenol oxidase.

Journal: Biochemical and biophysical research communications 20011207

Title: Partial purification, characterization, and histochemical localization of fully latent desert truffle (Terfezia claveryi Chatin) polyphenol oxidase.

Journal: Journal of agricultural and food chemistry 20010401

Title: Molecular mechanisms controlling the rate and specificity of catechol O-methylation by human soluble catechol O-methyltransferase.

Journal: Molecular pharmacology 20010201

Title: Proteolytic activation of latent Paraguaya peach PPO. Characterization of monophenolase activity.

Journal: Journal of agricultural and food chemistry 20010201

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Tags:4026-05-5 Molecular Formula|4026-05-5 MDL|4026-05-5 SMILES|4026-05-5 3-(tert-Butyl)benzene-1,2-diol