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Home Other Building Blocks 4-Bromobut-1-ene

4-Bromobut-1-ene

CAS No.:
5162-44-7
Catalog Number:
AG0035XQ
Molecular Formula:
C4H7Br
Molecular Weight:
135.0024
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$25
- +
100g
98%
In Stock USA
United States
$75
- +
500g
98%
In Stock USA
United States
$263
- +
Product Description
Catalog Number:
AG0035XQ
Chemical Name:
4-Bromobut-1-ene
CAS Number:
5162-44-7
Molecular Formula:
C4H7Br
Molecular Weight:
135.0024
MDL Number:
MFCD00000258
IUPAC Name:
4-bromobut-1-ene
InChI:
InChI=1S/C4H7Br/c1-2-3-4-5/h2H,1,3-4H2
InChI Key:
DMAYBPBPEUFIHJ-UHFFFAOYSA-N
SMILES:
BrCCC=C
EC Number:
225-937-4
Properties
Complexity:
24.8  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
133.973g/mol
Formal Charge:
0
Heavy Atom Count:
5  
Hydrogen Bond Acceptor Count:
0
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
135.004g/mol
Monoisotopic Mass:
133.973g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
0A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.1  
Literature
Title Journal
Photodissociation of 1-bromo-2-butene, 4-bromo-1-butene, and cyclopropylmethyl bromide at 234 nm studied using velocity map imaging. The Journal of chemical physics 20061014
Novel carbonyl bromoallylation/Heck reaction sequence. Stereocontrolled access to bicyclic beta-lactams. The Journal of organic chemistry 20050401
Thermal chemistry of C4 hydrocarbons on Pt(111): Mechanism for double-bond isomerization. The journal of physical chemistry. B 20050224
Straightforward asymmetric entry to highly functionalized 3-substituted 3-hydroxy-beta-lactams via Baylis-Hillman or bromoallylation reactions. The Journal of organic chemistry 20040206
Ion/molecule reactions of isomeric bromobutene radical cations with ammonia. European journal of mass spectrometry (Chichester, England) 20040101
DNA adducts of acrolein: site-specific synthesis of an oligodeoxynucleotide containing 6-hydroxy-5,6,7,8-tetrahydropyrimido[1,2-a]purin-10(3H)-one, an acrolein adduct of guanine. Chemical research in toxicology 20020501
Properties