sales@angenesci.com
Login | Register
logo
Structures Search
Home Other Building Blocks 4,4'-Di-tert-butylbiphenyl

4,4'-Di-tert-butylbiphenyl

CAS No.:
1625-91-8
Catalog Number:
AG001T70
Molecular Formula:
C20H26
Molecular Weight:
266.4204
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%(GC)
In Stock USA
United States
$43
- +
5g
98%(GC)
In Stock USA
United States
$57
- +
25g
98%(GC)
In Stock USA
United States
$178
- +
Product Description
Catalog Number:
AG001T70
Chemical Name:
4,4'-Di-tert-butylbiphenyl
CAS Number:
1625-91-8
Molecular Formula:
C20H26
Molecular Weight:
266.4204
MDL Number:
MFCD00008834
IUPAC Name:
1-tert-butyl-4-(4-tert-butylphenyl)benzene
InChI:
InChI=1S/C20H26/c1-19(2,3)17-11-7-15(8-12-17)16-9-13-18(14-10-16)20(4,5)6/h7-14H,1-6H3
InChI Key:
CDKCEZNPAYWORX-UHFFFAOYSA-N
SMILES:
CC(c1ccc(cc1)c1ccc(cc1)C(C)(C)C)(C)C
EC Number:
216-615-4
Properties
Complexity:
253  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
266.203g/mol
Formal Charge:
0
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
266.428g/mol
Monoisotopic Mass:
266.203g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
7.7  
Literature
Title Journal
Alkali metal reductions of organic molecules: why mediated electron transfer from lithium is faster than direct reduction. Journal of the American Chemical Society 20080917
[Treatment of 4, 4'-dBB in aqueous solution using O3/H2O2 system and its synergetic kinetics]. Huan jing ke xue= Huanjing kexue 20070901
The partial reduction of electron-deficient pyrroles: procedures describing both Birch (Li/NH3) and ammonia-free (Li/DBB) conditions. Nature protocols 20070101
The ammonia-free partial reduction of substituted pyridinium salts. Organic & biomolecular chemistry 20060321
Masked omega-lithio ester enolates: synthetic applications. Molecules (Basel, Switzerland) 20040430
The synthesis of homoallylic amines utilizing a cuprate-based 1,2-metalate rearrangement. The Journal of organic chemistry 20010126
Properties