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5162-44-7,MFCD00000258
Catalog No.:AA0035UY

5162-44-7 | 4-Bromobut-1-ene

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
98%
in stock  
$10.00   $7.00
- +
25g
98%
in stock  
$25.00   $17.00
- +
100g
98%
in stock  
$63.00   $44.00
- +
500g
98%
in stock  
$235.00   $164.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0035UY
Chemical Name:
4-Bromobut-1-ene
CAS Number:
5162-44-7
Molecular Formula:
C4H7Br
Molecular Weight:
135.0024
MDL Number:
MFCD00000258
SMILES:
BrCCC=C
Properties
Properties
 
BP:
99.3°C at 760 mmHg  
Form:
Liquid  
MP:
-115.07°C (estimate)  
Refractive Index:
n20/D 1.462(lit.)  
Solubility:
0.76g/l  
Stability:
Light Sensitive  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
24.8  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
5  
Hydrogen Bond Acceptor Count:
0  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2.1  

Synonyms
 
  
Literature

Title: Photodissociation of 1-bromo-2-butene, 4-bromo-1-butene, and cyclopropylmethyl bromide at 234 nm studied using velocity map imaging.

Journal: The Journal of chemical physics 20061014

Title: Novel carbonyl bromoallylation/Heck reaction sequence. Stereocontrolled access to bicyclic beta-lactams.

Journal: The Journal of organic chemistry 20050401

Title: Thermal chemistry of C4 hydrocarbons on Pt(111): Mechanism for double-bond isomerization.

Journal: The journal of physical chemistry. B 20050224

Title: Straightforward asymmetric entry to highly functionalized 3-substituted 3-hydroxy-beta-lactams via Baylis-Hillman or bromoallylation reactions.

Journal: The Journal of organic chemistry 20040206

Title: Ion/molecule reactions of isomeric bromobutene radical cations with ammonia.

Journal: European journal of mass spectrometry (Chichester, England) 20040101

Title: 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.

Journal: Chemical research in toxicology 20020501

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SDS
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Tags:5162-44-7 Molecular Formula|5162-44-7 MDL|5162-44-7 SMILES|5162-44-7 4-Bromobut-1-ene
Catalog No.: AA0035UY
5162-44-7,MFCD00000258
5162-44-7 | 4-Bromobut-1-ene
Pack Size： 10g
Purity： 98%
in stock
$10.00 $7.00
Pack Size： 25g
Purity： 98%
in stock
$25.00 $17.00
Pack Size： 100g
Purity： 98%
in stock
$63.00 $44.00
Pack Size： 500g
Purity： 98%
in stock
$235.00 $164.00
Quantity
- +
Add to Card
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bulk Quotation Request
Technical Information
Catalog Number: AA0035UY
Chemical Name: 4-Bromobut-1-ene
CAS Number: 5162-44-7
Molecular Formula: C4H7Br
Molecular Weight: 135.0024
MDL Number: MFCD00000258
SMILES: BrCCC=C
Properties
BP: 99.3°C at 760 mmHg  
Form: Liquid  
MP: -115.07°C (estimate)  
Refractive Index: n20/D 1.462(lit.)  
Solubility: 0.76g/l  
Stability: Light Sensitive  
Storage: Keep in dry area;2-8℃;  
Complexity: 24.8  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 5  
Hydrogen Bond Acceptor Count: 0  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2.1  
76:   
Literature fold

Title: Photodissociation of 1-bromo-2-butene, 4-bromo-1-butene, and cyclopropylmethyl bromide at 234 nm studied using velocity map imaging.

Journal: The Journal of chemical physics20061014

Title: Novel carbonyl bromoallylation/Heck reaction sequence. Stereocontrolled access to bicyclic beta-lactams.

Journal: The Journal of organic chemistry20050401

Title: Thermal chemistry of C4 hydrocarbons on Pt(111): Mechanism for double-bond isomerization.

Journal: The journal of physical chemistry. B20050224

Title: Straightforward asymmetric entry to highly functionalized 3-substituted 3-hydroxy-beta-lactams via Baylis-Hillman or bromoallylation reactions.

Journal: The Journal of organic chemistry20040206

Title: Ion/molecule reactions of isomeric bromobutene radical cations with ammonia.

Journal: European journal of mass spectrometry (Chichester, England)20040101

Title: 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.

Journal: Chemical research in toxicology20020501

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