+1 858-523-8231
Login | Register
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
Home Amines 1199-46-8
1199-46-8,MFCD00007698
Catalog No.:AA000PS5

1199-46-8 | 2-Amino-4-tert-butylphenol

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$7.00   $5.00
- +
25g
98%
in stock  
$13.00   $9.00
- +
100g
98%
in stock  
$26.00   $18.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA000PS5
Chemical Name:
2-Amino-4-tert-butylphenol
CAS Number:
1199-46-8
Molecular Formula:
C10H15NO
Molecular Weight:
165.2322
MDL Number:
MFCD00007698
SMILES:
Oc1ccc(cc1N)C(C)(C)C
NSC Number:
23803
Properties
Properties
 
BP:
274.9 °C at 760 mmHg  
Form:
Solid  
MP:
160-163 °C  
Refractive Index:
1.5290 (estimate)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
150  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
1  
XLogP3:
2.5  

Upstream Synthesis Route

[1]Patent:US4254118,1981,A,

[2]Patent:US4254121,1981,A,

[1]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2004,vol.43,#10,p.2243-2244

[2]Patent:US2429178,1944,,

[3]DokladyAkademiiNaukSSSR,1959,vol.125,p.1033,1034

[4]DokladyChemistry,124-129<1959>286,

[5]JournaloftheAmericanChemicalSociety,1958,vol.80,p.1662

[6]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2005,vol.44,#2,p.416-419

[7]BioorganicandMedicinalChemistry,2007,vol.15,#10,p.3515-3523

[1]JournaloftheAmericanChemicalSociety,1941,vol.63,p.308,309

[2]Diss.<Paris1939>S.16,

[3]JournalofOrganicChemistry,1954,vol.19,p.758,762,765

[1]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2005,vol.44,#2,p.416-419

[1]JournaloftheAmericanChemicalSociety,1995,vol.117,#34,p.8698-8706

Downstream Synthesis Route

[1]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2004,vol.43,p.2243-2244

[2]Patent:US2429178,1944,

[3]DokladyAkademiiNaukSSSR,1959,vol.125,p.1033,1034    DokladyChemistry,124-129<1959>286,

[4]JournaloftheAmericanChemicalSociety,1958,vol.80,p.1662

[5]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2005,vol.44,p.416-419

[6]BioorganicandMedicinalChemistry,2007,vol.15,p.3515-3523

[7]Molecularcatalysis,2020,vol.486

[1]Patent:FR1516276,1968,    Chem.Abstr.,1969,vol.70

636-94-2    1199-46-8   
2,5-bis(5-t-butyl-2-benzoxazolyl)phenol 

[1]JournalofHeterocyclicChemistry,1993,vol.30,p.1613-1622

5870-38-2    1199-46-8   
2,5-dihydroxy-1,4-di(5-tert-butylbenzoxazol-2-yl)benzene 

[1]ChemistryofHeterocyclicCompounds,1993,vol.29,p.212-215    KhimiyaGeterotsiklicheskikhSoedinenii,1993,p.242-245

[1]JournaloftheChemicalSociety.PerkinTransactions2(2001),1998,p.401-406

[2]Organometallics,2010,vol.29,p.89-100

Literature

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

Title: Modulation of alpha-synuclein aggregation by dopamine analogs.

Journal: PloS one 20100101

Title: 5-tert-Butyl-2-[5-(5-tert-butyl-1,3-benzoxazol-2-yl)-2-thien-yl]-1,3-benzoxazole.

Journal: Acta crystallographica. Section E, Structure reports online 20081201

Title: The h channel mediates location dependence and plasticity of intrinsic phase response in rat hippocampal neurons.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience 20080528

Title: [Substituted aminophenols and flavonoids as potential components for test-systems of total antioxidant activity].

Journal: Biomeditsinskaia khimiia 20070101

Title: Prediction of genotoxicity of chemical compounds by statistical learning methods.

Journal: Chemical research in toxicology 20050601

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

Journal: Biochemistry. Biokhimiia 20050301

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 1199-46-8
1220-78-6

1220-78-6

 1643-39-6

1643-39-6

 16523-28-7

16523-28-7

 91339-74-1

91339-74-1

 3535-88-4

3535-88-4

 16750-66-6

16750-66-6
Building Blocks
More >
Tags:1199-46-8 Molecular Formula|1199-46-8 MDL|1199-46-8 SMILES|1199-46-8 2-Amino-4-tert-butylphenol |Organic_Building_Blocks