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CAS No.: | 32451-95-9 |
---|---|
Name: | (Z)-dodec-3-en-1-ol |
Article Data: | 18 |
Molecular Structure: | |
Formula: | C12H24O |
Molecular Weight: | 184.322 |
Synonyms: | 3-Dodecen-1-ol,(Z)- (8CI);(Z)-3-Dodecen-1-ol;cis-3-Dodecen-1-ol; |
EINECS: | 251-057-5 |
Density: | 0.846 g/cm3 |
Boiling Point: | 268.1 °C at 760 mmHg |
Flash Point: | 97.6 °C |
PSA: | 20.23000 |
LogP: | 3.67560 |
dodec-3-yn-1-ol
(Z)-Dodec-3-en-1-ol
Conditions | Yield |
---|---|
With hydrogen; P-2 Ni In ethanol | 100% |
With hydrogen | 96% |
With quinoline; hydrogen; Lindlar's catalyst In hexane Ambient temperature; | 96% |
2-[((Z)-Dodec-3-enyl)oxy]-tetrahydro-pyran
(Z)-Dodec-3-en-1-ol
Conditions | Yield |
---|---|
With dowex In methanol at 45℃; | 89% |
With toluene-4-sulfonic acid In methanol at 20℃; for 16h; | 0.28 g |
(Z)-3-Dodecensaeure-ethylester
(Z)-Dodec-3-en-1-ol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether | 73% |
C
(Z)-Dodec-3-en-1-ol
D
(E)-3-dodecene-1-ol
Conditions | Yield |
---|---|
With ammonia; lithium In ethanol at -78℃; Title compound not separated from byproducts.; |
1-decyne
(Z)-Dodec-3-en-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) BuLi / 1.) HMPA, hexane, a) RT, 15 min, b) 50 deg C, 0.5 h, 2.) HMPA, hexane, a) RT, 1.5 h, b) 50 deg C, 2 h 2: 91 percent / H2, quinoline / Lindlar catalyst / hexane / 1 h / 10 °C View Scheme | |
Multi-step reaction with 4 steps 1: 1.) n-BuLi, 2.) HMPA / 1.) THF, -20 deg C, 0.5 h, 2.) THF, -78 deg C, 3 h 2: 84 percent / 2 N HCl / acetone / 6 h 3: 86 percent / NaBH4 4: 100 percent / H2 / P-2 Ni / ethanol View Scheme | |
Multi-step reaction with 2 steps 1: 1.) n-BuLi / 1.) THF/HMPA 2: H2 / Lindlar cat. / hexane View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) LiNH2, NH3 / 1.) THF, 45 min, 2.) THF, 5 h 2: 96 percent / H2, quinoline / 5percent Pd/CaCO3 / hexane / Ambient temperature View Scheme |
caprinaldehyde
(Z)-Dodec-3-en-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1: 63 percent / piperidine / xylene / Heating 2: 83 percent / LAH / diethyl ether 3: Br2 / CCl4 4: NaNH2 / CCl4; aq. NH3 / 4 h / -78 °C 5: 100 percent / H2 / P-2 Ni / ethanol View Scheme | |
Multi-step reaction with 3 steps 1: tetrahydrofuran / 0 - 20 °C 2: hydrogenchloride / benzene 3: 4,4'-di-tert-butylbiphenyl; lithium / tetrahydrofuran / 0 - 20 °C View Scheme |
(E)-dodec-3-enoic acid
(Z)-Dodec-3-en-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1: 83 percent / LAH / diethyl ether 2: Br2 / CCl4 3: NaNH2 / CCl4; aq. NH3 / 4 h / -78 °C 4: 100 percent / H2 / P-2 Ni / ethanol View Scheme |
(E)-3-dodecene-1-ol
(Z)-Dodec-3-en-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: Br2 / CCl4 2: NaNH2 / CCl4; aq. NH3 / 4 h / -78 °C 3: 100 percent / H2 / P-2 Ni / ethanol View Scheme |
(Z)-Dodec-3-en-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: NaNH2 / CCl4; aq. NH3 / 4 h / -78 °C 2: 100 percent / H2 / P-2 Ni / ethanol View Scheme |
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The 3-Dodecen-1-ol, (3Z)-, with the CAS registry number 32451-95-9, is also known as (3Z)-Dodec-3-en-1-ol. Its EINECS registry number is 251-057-5. This chemical's molecular formula is C12H24O and molecular weight is 184.32. What's more, its IUPAC name is called (Z)-Dodec-3-en-1-ol.
Physical properties about 3-Dodecen-1-ol, (3Z)- are: (1)ACD/LogP: 4.80; (2)# of Rule of 5 Violations: 0; (3)#H bond acceptors: 1; (4)#H bond donors: 1; (5)#Freely Rotating Bonds: 10; (6)Polar Surface Area: 9.23 Å2; (7)Index of Refraction: 1.456; (8)Molar Refractivity: 59.23 cm3; (9)Molar Volume: 217.7 cm3; (10)Surface Tension: 30.9 dyne/cm; (11)Density: 0.846 g/cm3; (12)Flash Point: 97.6 °C; (13)Enthalpy of Vaporization: 58.77 kJ/mol; (14)Boiling Point: 268.1 °C at 760 mmHg; (15)Vapour Pressure: 0.00106 mmHg at 25 °C.
Preparation of 3-Dodecen-1-ol, (3Z)-: this chemical can be prepared by Dodec-3-yn-1-ol. This reaction needs reagent H2 and solvent methanol. The yield is 96 %.
Uses of 3-Dodecen-1-ol, (3Z)-: it is used to produce other chemicals. For example, it can react with Toluene-4-sulfonyl chloride to get (Z)-3-Dodecenyl p-toluenesulfonate. The reaction occurs with solvent pyridine at temperature of 2-5 °C. The reaction time is 20 hours.
You can still convert the following datas into molecular structure:
(1) SMILES: OCC\C=C/CCCCCCCC
(2) InChI: InChI=1S/C12H24O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h9-10,13H,2-8,11-12H2,1H3/b10-9-
(3) InChIKey: BDGQTWOHKASHQU-KTKRTIGZSA-N