Product Details
Reputable factory supply 2-BROMOOCTANOIC ACID 2623-82-7 in bulk at low price
- Molecular Formula: C8H15BrO2
- Molecular Weight: 223.11
- Appearance/Colour: COLORLESS TO YELLOW LIQUID
- Vapor Pressure: 0.000941mmHg at 25°C
- Refractive Index: n20/D 1.471(lit.)
- Boiling Point: 281.4 °C at 760 mmHg
- PKA: 2.97±0.21(Predicted)
- Flash Point: 124 °C
- PSA： 37.30000
- Density: 1.321 g/cm3
- LogP: 2.80490
2-BROMOOCTANOIC ACID(Cas 2623-82-7) Usage
|
General Description |
2-Bromooctanoic acid is an effective substitute for the expensive (2,000 times) and cell-growth-inhibiting polyhydroxyalkanoic acid synthesis inhibitor, cerulenin. It blocks the formation of polyhydroxyalkanoic acid in Pseudomonas fluorescens BM07 without any influence on the cell growth when grown on fructose. It inhibits β-oxidation of fatty acids in perfused rat liver and in mitochondria isolated from rat liver. |
InChI:InChI=1/C8H15BrO2/c1-2-3-4-5-6-7(9)8(10)11/h7H,2-6H2,1H3,(H,10,11)
2623-82-7 Relevant articles
The Stoichiometry and Promoter Role of Chlorosulfuric and Fuming Sulfuric Acids for α-Halogenation of Aliphatic Acid
Ogata, Yoshiro,Watanabe, Shinya
, p. 2417 - 2418 (1980)
The stoichiometry for the chlorosulfuric...
Synthesis and biological evaluation of novel N-α-haloacylated homoserine lactones as quorum sensing modulators
Syrpas, Michail,Ruysbergh, Ewout,Stevens, Christian V.,De Kimpe, Norbert,Mangelinckx, Sven
, p. 2539 - 2549 (2015/02/19)
Novel N-α-haloacylated homoserine lacton...
Enantioselective construction of tetrasubstituted stereogenic carbons through bronsted base catalyzed michael reactions: α′-hydroxy enones as key enoate equivalent
Badiola, Eider,Fiser, Bla,Gmez-Bengoa, Enrique,Mielgo, Antonia,Olaizola, Iurre,Urruzuno, Iaki,Garca, Jess M.,Odriozola, Jos M.,Razkin, Jess,Oiarbide, Mikel,Palomo, Claudio
supporting information, p. 17869 - 17881 (2015/02/19)
Catalytic and asymmetric Michael reactio...
Mesoionic 5-alkyl-1,3-dithiolium-4-thiolates: Synthesis and brine shrimp toxicity
De Almeida, Paulo Afonso,Da Silva, Tania Maria Sarmento,Echevarria, Aurea
, p. 593 - 600 (2007/10/03)
A series of twelve 1,3-dithiolium-4-thio...
N-hdroxy-2-(alkyl, aryl, or heteroaryl, sulfanyl, sulfinyl or sulfonyl)-3-substituted alkyl, aryl or heteroarylamides as matrix metalloproteinase inhibitors
-
, (2008/06/13)
Matrix metalloproteinases (MMPs) are a g...
2623-82-7 Process route
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124-07-2
Octanoic acid
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2623-82-7,70610-87-6
2-bromooctanoic acid
| Conditions | Yield |
|---|---|
|
With
thionyl chloride; bromine; sodium hydroxide;
at 20 ℃;
Reflux;
|
67%
|
|
With
bromine; phosphorus trichloride;
at 65 - 100 ℃;
for 5h;
|
56%
|
|
With
chlorosulfonic acid; bromine;
In
diethyl ether; 1,2-dichloro-ethane;
at 80 ℃;
for 2h;
Mechanism;
other halogen, promoter, concentrations, other acids;
|
|
|
With
bromine; phosphorus tribromide;
|
|
|
With
phosphorus; bromine;
und nachfolgendem Behandeln mit Wasser;
|
|
|
With
bromine; phosphorus trichloride;
|
|
|
With
bromine; phosphorus trichloride;
at 80 - 100 ℃;
for 15h;
|
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78389-69-2
(2-Bromo-octyloxy)-trimethyl-silane
-
-
2623-82-7,70610-87-6
2-bromooctanoic acid
| Conditions | Yield |
|---|---|
|
With
chromium(VI) oxide; sulfuric acid;
In
dichloromethane;
at 0 ℃;
for 0.75h;
Yield given;
|
2623-82-7 Upstream products
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124-07-2
Octanoic acid
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78389-69-2
(2-Bromo-octyloxy)-trimethyl-silane
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111-64-8
n-octanoic acid chloride
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2984-50-1
1,2-Epoxyoctane
2623-82-7 Downstream products
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644-90-6
2-aminooctanoic acid
-
102006-16-6
2-Benzaminooxy-octansaeure-(1)
-
5815-35-0
7,8-dicarboxytetradecane
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821-95-4
1-undecene