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3140-93-0

3140-93-0 | 2,3-Dibromothiophene

CAS No: 3140-93-0 Catalog No: AG0032XL MDL No:MFCD00005418

Product Description

Catalog Number:
AG0032XL
Chemical Name:
2,3-Dibromothiophene
CAS Number:
3140-93-0
Molecular Formula:
C4H2Br2S
Molecular Weight:
241.9317
MDL Number:
MFCD00005418
IUPAC Name:
2,3-dibromothiophene
InChI:
InChI=1S/C4H2Br2S/c5-3-1-2-7-4(3)6/h1-2H
InChI Key:
ATRJNSFQBYKFSM-UHFFFAOYSA-N
SMILES:
Brc1sccc1Br
EC Number:
221-542-6
NSC Number:
99003

Properties

Complexity:
66.7  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
241.822g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
241.928g/mol
Monoisotopic Mass:
239.824g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
28.2A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.5  

Literature

Title Journal
Synthesis of di-, tri-, and tetrasulfides through multifold carbon-sulfur cross-coupling reactions with indium tri(organothiolates) in a one-pot procedure. The Journal of organic chemistry 20110204
A three-step synthetic approach to asymmetrically functionalized 4H-cyclopenta[2,1-b:3,4-b']dithiophenes. The Journal of organic chemistry 20101105
Facile synthesis of a family of H8BINOL-amine compounds and catalytic asymmetric arylzinc addition to aldehydes. The Journal of organic chemistry 20100507
3,3',5,5'-Tetra-bromo-2,2'-bithio-phene. Acta crystallographica. Section E, Structure reports online 20090501
Prediction of genotoxicity of chemical compounds by statistical learning methods. Chemical research in toxicology 20050601
NMR quantum computing: applying theoretical methods to designing enhanced systems. Magnetic resonance in chemistry : MRC 20041001
Synthesis of 2,3-substituted thienylboronic acids and esters. The Journal of organic chemistry 20031128

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