.png)
2-HEPTENOIC ACID
Base Information
- Chemical Name: 2-HEPTENOIC ACID
- CAS No.: 10352-88-2
Manufacturer supply good quality 2-HEPTENOIC ACID 10352-88-2 with stock
- Molecular Formula: C7H12 O2
- Molecular Weight: 128.171
- Vapor Pressure: 0.0295mmHg at 25°C
- Melting Point: -19°C (estimate)
- Refractive Index: 1.4288 (estimate)
- Boiling Point: 226.6°C at 760 mmHg
- PKA: 4.79±0.10(Predicted)
- Flash Point: 133.4°C
- PSA： 37.30000
- Density: 0,955 g/cm3
- LogP: 1.81740
2-HEPTENOIC ACID(Cas 10352-88-2) Usage
|
Definition |
ChEBI: A 2-heptenoic acid having the trans configuration. |
InChI:InChI=1/C7H12O2/c1-2-3-4-5-6-7(8)9/h5-6H,2-4H2,1H3,(H,8,9)/b6-5+
10352-88-2 Relevant articles
Co-catalysis over a tri-functional ligand modified Pd-catalyst for hydroxycarbonylation of terminal alkynes towards α,β-unsaturated carboxylic acids
Yang, Da,Liu, Huan,Liu, Lei,Guo, Wen-Di,Lu, Yong,Liu, Ye
, p. 5336 - 5344 (2019)
An amphiphilic tri-functional ligand (L1...
Inhibition of human cytochrome P450 2E1 and 2A6 by aldehydes: Structure and activity relationships
Kandagatla, Suneel K.,Mack, Todd,Simpson, Sean,Sollenberger, Jill,Helton, Eric,Raner, Gregory M.
, p. 195 - 202 (2014)
The purpose of this study was to probe a...
Direct reaction of dibromoacetic acid with aldehydes promoted by samarium diiodide: An easy, efficient, and rapid synthesis of (E)-α,β- unsaturated carboxylic acids with total stereoselectivity
Concellon, Jose M.,Concellon, Carmen
, p. 1728 - 1731 (2006)
A promoted SmI2 direct reaction of dibro...
-
Zweifel,Backlund
, p. 3184 (1977)
-
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...
COMPOUNDS FOR USE AS AN ANTI-BACTERIAL OR ANTI-FUNGAL AGENT AND AS A ZINC SENSOR
-
Paragraph 0107; 0108; 0109, (2018/01/18)
The present invention relates to a compo...
MANUFACTURING METHOD OF α,β-UNSATURATED CARBOXYLIC ACID
-
Paragraph 0050-0052, (2018/10/16)
PROBLEM TO BE SOLVED: To provide a manuf...
10352-88-2 Process route
-
-
110-62-3
pentanal
-
-
141-82-2
malonic acid
-
-
10352-88-2
E-hept-2-enoic acid
| Conditions | Yield |
|---|---|
|
With
piperidine; pyridine;
at 20 - 45 ℃;
for 24h;
|
86%
|
|
With
pyridine;
|
71%
|
|
With
pyrrolidine; pyridine;
for 0.5h;
Reflux;
|
65%
|
|
|
45%
|
|
Multistep reaction;
(i) Py, (ii) (decarboxylation);
|
-
-
18829-55-5
(E)-2-Heptenal
-
-
10352-88-2
E-hept-2-enoic acid
| Conditions | Yield |
|---|---|
|
With
sodium chlorite; sodium dihydrogen phosphate monohydrate; 2-methyl-but-2-ene;
In
water; tert-butyl alcohol;
at 20 ℃;
for 12h;
|
84%
|
|
With
human P4502E1 supersomes; NADPH;
In
aq. phosphate buffer;
at 37 ℃;
for 0.75h;
pH=7.4;
Reagent/catalyst;
Enzymatic reaction;
|
10352-88-2 Upstream products
-
592-41-6
1-hexene
-
110-62-3
pentanal
-
141-82-2
malonic acid
-
1483-67-6
hept-2-ynoic acid
10352-88-2 Downstream products
-
81002-21-3
(E)-Hept-2-enoic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
-
76875-23-5
(E)-Hept-2-enoyl chloride
-
1025980-48-6
3-cyclohexylsulfanyl-heptanoic acid
-
851228-11-0
3-(4-methoxy-phenylsulfanyl)-heptanoic acid