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Home Other Building Blocks 1625-91-8
1625-91-8,MFCD00008834
Catalog No.:AA001T48

1625-91-8 | 4,4'-Di-tert-butylbiphenyl

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5g
97%
in stock  
$7.00   $5.00
- +
10g
97%
in stock  
$9.00   $7.00
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25g
97%
in stock  
$22.00   $15.00
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100g
97%
in stock  
$35.00   $25.00
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500g
97%
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$172.00   $121.00
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  • 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:
AA001T48
Chemical Name:
4,4'-Di-tert-butylbiphenyl
CAS Number:
1625-91-8
Molecular Formula:
C20H26
Molecular Weight:
266.4204
MDL Number:
MFCD00008834
SMILES:
CC(c1ccc(cc1)c1ccc(cc1)C(C)(C)C)(C)C
Properties
Properties
 
BP:
337.8°C at 760 mmHg  
Form:
Solid  
MP:
126-130 °C(lit.);  
Refractive Index:
1.5928 (estimate)  
Solubility:
dioxane: 0.1 g/mL, clear  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
253  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
20  
Rotatable Bond Count:
3  
XLogP3:
7.7  

Upstream Synthesis Route

[1]JournalofOrganicChemistry,1979,vol.44,p.3037-3041

[1]ChemistryLetters,1983,p.1201-1202

[1]RecueildesTravauxChimiquesdesPays-Bas,1995,vol.114,#7,p.311-316

[1]JournalofOrganicChemistry,2004,vol.69,#16,p.5476-5479

Downstream Synthesis Route

[1]ZhurnalObshcheiKhimii,1958,vol.28,p.413,416;engl.Ausg.S.405,407

[1]JournalofOrganicChemistry,2005,vol.70,p.5014-5019

[2]JournalofOrganicChemistry,1979,vol.44,p.3037-3041

[3]Patent:US2015/291713,2015,A1

[1]Patent:US2007/293708,2007,A1.Locationinpatent:Page/Pagecolumn1

[2]MonatsheftefurChemie,2012,vol.143,p.683-686

[3]Patent:CN106220514,2016,A.Locationinpatent:Paragraph0107;0114;0115;0116

[4]Macromolecules,2005,vol.38,p.7950-7956

[5]AngewandteChemie-InternationalEdition,2011,vol.50,p.12582-12585

[6]JournalofOrganicChemistry,1979,vol.44,p.3037-3041

[7]Patent:WO2006/93466,2006,A1.Locationinpatent:Page/Pagecolumn38;Sheet13

[8]Tetrahedron,2008,vol.64,p.10814-10820

[9]Organicelectronics,2012,vol.13,p.1553-1564

[10]DyesandPigments,2015,vol.121,p.7-12

[1]JournalofOrganicChemistry,1979,vol.44,p.3037-3041

[2]OrganicLetters,2019,vol.21,p.7004-7008

[1]JournalofOrganicChemistry,1979,vol.44,p.3037-3041

Literature

Title: Alkali metal reductions of organic molecules: why mediated electron transfer from lithium is faster than direct reduction.

Journal: Journal of the American Chemical Society 20080917

Title: [Treatment of 4, 4'-dBB in aqueous solution using O3/H2O2 system and its synergetic kinetics].

Journal: Huan jing ke xue= Huanjing kexue 20070901

Title: The partial reduction of electron-deficient pyrroles: procedures describing both Birch (Li/NH3) and ammonia-free (Li/DBB) conditions.

Journal: Nature protocols 20070101

Title: The ammonia-free partial reduction of substituted pyridinium salts.

Journal: Organic & biomolecular chemistry 20060321

Title: Masked omega-lithio ester enolates: synthetic applications.

Journal: Molecules (Basel, Switzerland) 20040430

Title: The synthesis of homoallylic amines utilizing a cuprate-based 1,2-metalate rearrangement.

Journal: The Journal of organic chemistry 20010126

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SDS
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