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Detail of "1625-91-8"

  • MSDS Download
  • CAS Number:
  • 1625-91-8
  • Name:
  • 1,1'-Biphenyl,4,4'-bis(1,1-dimethylethyl)-

  • Superlist Name:
  • 4,4'-Di-tert-butylbiphenyl
  • Molecular Structure:
  • Formula:
  • C20H26
  • Molecular Weight:
  • 266.4204
  • Synonyms:
  • Biphenyl,4,4'-di-tert-butyl- (6CI,7CI,8CI);4,4'-Bis(1,1-dimethylethyl)-1,1'-biphenyl;4,4'-Di-tert-butyl-1,1'-biphenyl;4,4'-Di-tert-butylbiphenyl;p,p'-Di-tert-butylbiphenyl;
  • EINECS:
  • 216-615-4
  • Density:
  • 0.924 g/cm3
  • Melting Point:
  • 126-130 °C(lit.)
  • Boiling Point:
  • 337.8 °C at 760 mmHg
  • Flash Point:
  • 173.9 °C
  • Solubility:
  • dioxane: 0.1 g/mL, clear
  • Appearance:
  • WHITE POWDER, CRYSTALS, CRYSTALLINE POWDER AND/OR CHUNKS

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CAS No.1625-91-8 4,4'-Di-tert-butylbiphenyl

Supplier:KindChem Co.,Ltd, [ China (Mainland)]

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CAS No.1625-91-8 4,4'-Di-tert-butylbiphenyl

Supplier:Shanghai Chainpharm Bio-medical Technology CO.,Ltd [ China (Mainland)]

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Address:Rm.403 Building A2,No. 688,Qiushi Rd,Jinshan District,Shanghai.China

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CAS No.1625-91-8 4,4'-Di-tert-butylbiphenyl

Supplier:UAB Tikslioji Sinteze [ Lithuania]

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589Integral
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Address:Kalvariju g. 201E

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CAS No.1625-91-8 4,4'-Di-tert-butylbiphenyl

Assay:99%

TIMTEC-BB SBB007812;4,4’-DI-T-BUTYLBIPHENYL;4,4’-Di-t-butylbiphenyl;4,4’-DI-TERT-BUTYLBIPHENYL;4,4’-Ditert-butyl-1,1’-biphenyl;4,4’-Di-tert-butylbiphenyl, 99+%;4,4’-Di-tert-butylbiphenyl Zone Refined;1,1’-Biphenyl, 4,4’-bis(1,1-dimethylethyl)-;4,4’-Di-tert-butylbiphenyl Zone Refi

Min. Order:1Gram

Supplier:Beijing BangGui Drug Research Ltd. [ China (Mainland)]

115Integral
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Tel:+86-010-56201763

Address:XiaoliZhuang 66,Changping District,Beijing,China.

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CAS No.1625-91-8 4,4'-Di-tert-butylbiphenyl

4,4'-DI-TERT-BUTYLBIPHENYL

Supplier:DALCHEM [ Russian Federation]

610Integral
610

Tel:+7 (8312) 75-37-72, 75-49-58

Address:Moskovskoe shosse 85, N.Novgorod 603079, Russia

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CAS No.1625-91-8 4,4'-Di-tert-butylbiphenyl

Supplier:Beijing zhongke expanding chemical technology Co., LTD. [ China (Mainland)]

600Integral
600

Tel:010-51600645 58608265;57131961

Address:Beijing changping area connects center north pearl tower 2 buildings

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Reference

Lithiated benzyllithiums from chlorobenzyl chlorides by a DTBB-catalyzed lithiation
Lithiated benzyllithiums from chlorobenzyl chlorides by a DTBB-catalyzed lithiation. Gomez, Cecilia; Huerta, Fernando F.; Yus, Miguel (Facultad Ciencias, Univ. Alicante, Alicante E-03080, Spain). Tetrahedron Letters, 38(4), 687-690 (English) 1997 Elsevier. CODEN: TELEAY. ISSN: 0040-4039. DOCUMENT TYPE: Journal CA Section: 25 (Benzene, Its Derivatives, and Condensed Benzenoid Compounds) The reaction of 2-, 3- or 4-chlorobenzyl chlorides with an excess of lithium and a catalytic amt. of DTBB (7 mol%) in the presence of different electrophiles [Me2CHCHO, tert-BuCHO, Et2CO, (CH2)5CO, PhCOMe, Me3SiCl] in THF at -50°C leads after hydrolysis with water, to the expected diols or disilylated compds.In this experiment, several chemicals are used like 187274-03-9 and 1625-91-8 EC6H4E [ E = Me2CHCHOH, Me3CCHOH, Et2COH, (CH2)5COH, PhC(OH)Me, Me3Si]. .
b-Functionalized organolithium compounds through a sulfur-lithium exchange
b-Functionalized organolithium compounds through a sulfur-lithium exchange. Foubelo, Francisco; Gutierrez, Ana; Yus, Miguel (Departamento de QUimica Organica, Facultad de Ciencias, Universidad de Alicante, Alicante E-03080, Spain).In this study,1625-91-8 is also used. Tetrahedron Letters, 38(27), 4837-4840 (English) 1997 Elsevier. CODEN: TELEAY. ISSN: 0040-4039. DOCUMENT TYPE: Journal CA Section: 21 (General Organic Chemistry) The successive reaction of b-hydroxy or b-amino thioethers HYCHR1CH2SPh (Y = O, NPh; R1 = H, Ph, n-C6H13) with n-butyllithium and an excess of lithium powder and a catalytic amt. of DTBB (4,4'-di-tert-butylbiphenyl) in THF at -78°C leads to the formation of the corresponding b-functionalized organolithium compds. LiYCHR1CH2Li, which by reaction with electrophiles [D2O, ButCHO, PhCHO, Me2CO, (CH2)5CO] at temps. ranging between -78 and 20°C yields, after hydrolysis with water, the expected functionalized alcs. or amines HYCHR1CH2E [E = D, ButCH(OH), etc.] in a regioselective manner. .
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