TRANS-2-OCTENOIC ACID
Base Information
- Chemical Name: TRANS-2-OCTENOIC ACID
- CAS No.: 1871-67-6
Factory sells TRANS-2-OCTENOIC ACID 1871-67-6 with sufficient production capacity
- Molecular Formula: C8H14O2
- Molecular Weight: 142.198
- Appearance/Colour: CLEAR COLOURLESS TO SLIGHTLY YELLOW LIQUID
- Vapor Pressure: 0.0037mmHg at 25°C
- Melting Point: 5-6 °C(lit.)
- Refractive Index: n20/D 1.4588(lit.)
- Boiling Point: 260.2 °C at 760 mmHg
- PKA: 4.78±0.10(Predicted)
- Flash Point: 151.1 °C
- PSA: 37.30000
- Density: 0.955 g/cm3
- LogP: 2.20750
TRANS-2-OCTENOIC ACID(Cas 1871-67-6) Usage
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Synthesis Reference(s) |
Tetrahedron Letters, 31, p. 4719, 1990 DOI: 10.1016/S0040-4039(00)97715-3 |
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Definition |
ChEBI: An olefinic fatty acid that is octanoic acid carrying a double bond at position 2 (the 2E-isomer). |
InChI:InChI=1/C8H14O2/c1-2-3-4-5-6-7-8(9)10/h6-7H,2-5H2,1H3,(H,9,10)/p-1
1871-67-6 Relevant articles
Reaction of a lysyl residue analogue with E-2-octenal
Alaiz, Manuel,Barragan, Santiago
, p. 43 - 50 (1995)
The reaction of E-2-octenal and N2-(carb...
Ligand-controlled divergent dehydrogenative reactions of carboxylic acids via C–H activation
Wang, Zhen,Hu, Liang,Chekshin, Nikita,Zhuang, Zhe,Qian, Shaoqun,Qiao, Jennifer X.,Yu, Jin-Quan
, p. 1281 - 1285 (2021/12/10)
Dehydrogenative transformations of alkyl...
Carboxylation of Alkenyl Boronic Acids and Alkenyl Boronic Acid Pinacol Esters with CO2 Catalyzed by Cuprous Halide
Hong, Junting,Nayal, Onkar S.,Mo, Fanyang
supporting information, p. 2813 - 2818 (2020/05/16)
A cuprous halide catalysed carboxylation...
Method for preparing alpha, beta-unsaturated carboxylic acid by reacting alkenyl boron compound with carbon dioxide under catalysis of cuprous halide
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Paragraph 0061-0062, (2020/06/17)
The invention discloses a method for pre...
Preparation method of (E, Z)-2, 4-ethyl decadienoate
-
Paragraph 0040; 0041, (2019/05/15)
The invention provides a preparation met...
1871-67-6 Process route
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-
4360-85-4
hexylidene-malonic acid
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-
1871-67-6
(E)-oct-2-enoic acid
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-
1577-19-1
2-hexen-1-yl acetate
| Conditions | Yield |
|---|---|
|
With
pyridine;
at 0 - 20 ℃;
Inert atmosphere;
|
79%
|
-
-
141-82-2
malonic acid
-
-
66-25-1
hexanal
-
-
1871-67-6
(E)-oct-2-enoic acid
-
-
1577-19-1
2-hexen-1-yl acetate
| Conditions | Yield |
|---|---|
|
With
pyrrolidine; pyridine;
at 0 - 20 ℃;
stereoselective reaction;
Inert atmosphere;
|
89%
|
1871-67-6 Upstream products
-
18402-83-0
(E)-non-3-en-2-one
-
1577-96-4
(Z)-oct-2-enoic acid
-
18088-13-6
1,1,1,3-tetrachlorooctane
-
141-82-2
malonic acid
1871-67-6 Downstream products
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18409-17-1
(E)-oct-2-en-1-ol
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1026421-26-0
3-phenylsulfanyl-octanoic acid
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7367-81-9
methyl (E)-oct-2-enoate
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2548-87-0
(E)-2-Octenal