Alpha beta-unsaturated carbonyl compounds

Alpha beta-unsaturated carbonyl compounds

Alpha beta-unsaturated carbonyl compounds are classes of organic compounds made of double-bonded carbon atoms (alkene) near a carbon double-bonded to an oxygen atom and single-bonded with other atoms (ketone).
100°C (0.1 mmHg)(sublimation) (3)
101°C to 102°C (5.0 mmHg) (2)
101.0°C to 103.0°C (1)
103°C to 104°C (7)
115°C to 118°C (2)
115.0°C to 125.0°C (2)
117°C to 119°C (2)
119°C to 121°C (2)
125°C (2)
125°C to 126°C (13 mmHg) (1)
126°C to 128°C (12 mmHg) (2)
127°C to 129°C (2)
129°C (2)
129°C to 130°C (4)
132.0°C to 133.0°C (2)
133°C (2)
134°C to 136°C (3)
134.0°C to 136.0°C (2)
135°C to 137°C (2)
136°C (2)
136°C to 139°C (2)
138°C to 140°C (1)
140°C to 142°C (15 mmHg) (2)
150°C (2)
150°C (0.05 mmHg) (2)
156°C (2)
169°C to 171°C (2)
180°C (0.1 mmHg)(sublimation) (2)
184°C to 188°C (2)
185°C to 188°C (15 mmHg) (2)
200°C (2)
205°C (2)
205°C (0.1 mmHg)(sublimation) (2)
209°C to 213°C (2)
220°C (11.0 mmHg) (3)
220°C (decomposition) (1)
237°C (2)
237.0°C to 239.0°C (3)
249°C (15.0 mmHg) (1)
270°C to 273°C (2)
300°C (decomposition) (3)
32°C to 34°C (60 mm) (1)
32°C to 34°C (60 mmHg) (2)
340°C (4)
370°C (decomposition) (2)
51.0°C to 53.0°C (12.0 mmHg) (1)
52°C (75 mmHg) (2)
56°C to 60°C (16 mmHg) (2)
60°C (16 mmHg) (3)
65°C (15 mmHg) (2)
66°C to 69°C (12 mmHg) (3)
67°C to 68°C (50 mmHg) (2)
69°C to 70°C (2)
69.0°C (5)
70.0°C (75.0 mmHg) (2)
75°C to 76°C (0.8 mmHg) (2)
75°C to 76°C (1.1 hPa) (2)
78.0°C to 81.0°C (14.0 mmHg) (1)
80°C to 82°C (1 mmHg) (2)
84°C to 86°C (3)
85°C (12 mmHg) (3)
85.0°C (2)
90°C to 110°C (0.1 mmHg)(sublimation) (2)
92°C to 93°C (3)
92°C to 93°C (10 mmHg) (3)
95°C to 96°C (20 mmHg) (2)
Reacton™ (2)
Technical (14)
100.12 (5)
1040.52 (3)
1058.584 (2)
112.17 (6)
113.16 (2)
114.14 (1)
122.10 (3)
124.183 (2)
126.199 (9)
128.127 (2)
140.23 (3)
142.198 (2)
144.17 (2)
144.173 (2)
146.189 (3)
156.18 (2)
156.3 (2)
168.12 (1)
185.223 (1)
188.23 (2)
192.30 (5)
192.302 (2)
215.073 (1)
238.30 (2)
240.178 (2)
253.16 (3)
256.91 (7)
258.12 (3)
265.16 (3)
303.135 (1)
310.20 (2)
330.59 (1)
347.35 (1)
348.27 (3)
349.32 (4)
393.30 (3)
400.23 (3)
405.418 (2)
406.62 (2)
412.15 (3)
425.24 (2)
425.48 (3)
430.09 (3)
470.37 (2)
477.65 (1)
487.66 (2)
515.09 (2)
574.92 (3)
608.682 (3)
68.08 (5)
691.742 (2)
70.09 (11)
70.091 (2)
704.801 (2)
707.06 (2)
708.74 (1)
722.867 (2)
758.793 (2)
828.34 (2)
84.118 (13)
84.12 (9)
915.73 (4)
96.129 (2)
98.14 (6)
98.145 (9)
98.15 (4)
99.13 (2)
99.133 (2)
≥90% (8)
≥98% (4)
85% (2)
90% (18)
94% (2)
95% (13)
96% (23)
97% (48)
97% (typically) (3)
98% (34)
99% (15)
99+% (1)
99.9% (13)
99.99% (4)
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Tris(dibenzylideneacetone)dipalladium(0) is the most widely used Pd0 precursor complex in synthesis and catalysis, in particular as a catalyst for various coupling reactions. It is used as a catalyst precursor for palladium-catalyzed carbon-nitrogen bond formation, conversion of aryl chlorides,...
 
Tiglic aldehyde was used in the concise total synthesis of 7-demethylpiericidin A11. It was used as starting reagent during the synthesis of alkyl-branched tetraene hydrocarbons, pheromone component for dried fruit beetle.
4-Amino-3-penten-2-one, 96% 
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo...
 
6-Methyl-3,5-heptadien-2-one is used in the preparation of (RS)-(E)-2,6-dimethyl-1,2-epoxy-3,5-heptadiene. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand.
 
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo...
 
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo...
 
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo...
 
It is used as pharmaceutical intermediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand.
 
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo...
 
This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to...
 
It is used in most dairy flavors to add greater depth. This ketone will add lingering rich after-notes, to many processed dairy products such as custard, melted butter, creams and cheeses (Brie, Gorgonzola and blue cheeses). Also beneficial in fatty nut applications (brazil and pine nuts, cashews).
 
Sodium 2,4-pentanedionate hydrate is used as a pharmaceutical intermediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand.
 
This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to...
 
This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to...
4-Methyl-2-pentenal, 95% 
This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to...
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Meerwein Arylation
In 1939, German chemist Hans Meerwein and colleagues studied the reaction of diazo compounds with alpha, beta-unsaturated carbonyl compounds, in which the aryl group was added across the double bond and a molecule of nitrogen was lost.
Hydrides
To inorganic chemists, hydrides are compounds or ions made up of hydrogen bonded to an electropositive (or a less electronegative) element. Hydrides can be formed with almost all main-group elements, but inorganic hydrides are usually classified iinto four main groups: covalent, ionic, transition...
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Molecular Probes Handbook
Reagents for Modifying Aldehydes and Ketones—Section 3.3
Molecular Probes Handbook
Probes for Lipid Metabolism and Signaling—Section 17.4
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