Basic Information | Post buying leads | Suppliers | Cas Database |
Name |
11-Hexadecen-1-ol, (11E)- |
EINECS | 262-704-6 |
CAS No. | 61301-56-2 | Density | 0.847 g/cm3 |
PSA | 20.23000 | LogP | 5.23600 |
Solubility | N/A | Melting Point |
N/A |
Formula | C16H32O | Boiling Point | 309 °C at 760 mmHg |
Molecular Weight | 240.429 | Flash Point | 134.9 °C |
Transport Information | N/A | Appearance | N/A |
Safety | Risk Codes | N/A | |
Molecular Structure | Hazard Symbols | N/A | |
Synonyms |
11-Hexadecen-1-ol,(E)-;(E)-11-Hexadecen-1-ol;(E)-11-Hexadecenol;trans-11-Hexadecen-1-ol; |
Article Data | 6 |
(E)-11-hexadecen-1-yl acetate
trans-11-hexadecen-1-ol
Conditions | Yield |
---|---|
With sodium hydroxide In ethanol for 0.5h; Ambient temperature; | 97% |
1-(2-tetrahydropyranyloxy)-11E-hexadecene
trans-11-hexadecen-1-ol
Conditions | Yield |
---|---|
With pyridinium p-toluenesulfonate In methanol at 45℃; for 3h; | 92% |
8-phenylsulfonyl-11E-hexadecen-1-ol
trans-11-hexadecen-1-ol
Conditions | Yield |
---|---|
With ammonia; lithium In tetrahydrofuran at -60℃; for 1h; | 61% |
11-hexadecyn-1-ol
trans-11-hexadecen-1-ol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In tetrahydrofuran; diethylene glycol dimethyl ether at 140℃; for 48h; | 56.3% |
With lithium aluminium tetrahydride In diethylene glycol dimethyl ether at 130℃; for 5h; | 1.1 g |
pentanal
(11‑hydroxyundecyl)triphenylphosphonium bromide
A
(Z)-11-hexadecen-1-ol
B
trans-11-hexadecen-1-ol
Conditions | Yield |
---|---|
With sodium hydride; dimethyl sulfoxide In tetrahydrofuran for 0.5h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; |
10-chlorodecanol
trans-11-hexadecen-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) lithium amide / 1.) HMPTA, RT, 1.5 h, 2.) HMPTA, 25 deg C, 8 h 2: 56.3 percent / LiAlH4 / bis-(2-methoxy-ethyl) ether; tetrahydrofuran / 48 h / 140 °C View Scheme |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) lithium amide / 1.) HMPTA, RT, 1.5 h, 2.) HMPTA, 25 deg C, 8 h 2: 56.3 percent / LiAlH4 / bis-(2-methoxy-ethyl) ether; tetrahydrofuran / 48 h / 140 °C View Scheme |
1-Bromo-11-hydroxyundecane
trans-11-hexadecen-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 90 percent / acetonitrile 2: DMSO, NaH / tetrahydrofuran / 0.5 h View Scheme |
1-bromohexyne
trans-11-hexadecen-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) ThxBHCl*Me2S, 2.) KIPBH, 3.) NaOMe, 4.) AcOH 2: 97 percent / 20percent aq. NaOH / aq. ethanol / 0.5 h / Ambient temperature View Scheme |
9-decen-1-yl acetate
trans-11-hexadecen-1-ol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 1.) ThxBHCl*Me2S, 2.) KIPBH, 3.) NaOMe, 4.) AcOH 2: 97 percent / 20percent aq. NaOH / aq. ethanol / 0.5 h / Ambient temperature View Scheme |
This chemical is called 11-Hexadecen-1-ol, (11E)-, and its systematic name is (11E)-hexadec-11-en-1-ol. With the molecular formula of C16H32O, its molecular weight is 240.42. The CAS registry number of this chemical is 61301-56-2.
Other characteristics of the 11-Hexadecen-1-ol, (11E)- can be summarised as followings: (1)ACD/LogP: 6.73; (2)# of Rule of 5 Violations: 1; (3)ACD/LogD (pH 5.5): 6.73; (4)ACD/LogD (pH 7.4): 6.73; (5)ACD/BCF (pH 5.5): 77122.36; (6)ACD/BCF (pH 7.4): 77122.36; (7)ACD/KOC (pH 5.5): 109603.27; (8)ACD/KOC (pH 7.4): 109603.27; (9)#H bond acceptors: 1; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 14; (12)Polar Surface Area: 9.23 Å2; (13)Index of Refraction: 1.46; (14)Molar Refractivity: 77.76 cm3; (15)Molar Volume: 283.7 cm3; (16)Polarizability: 30.8×10-24cm3; (17)Surface Tension: 31.5 dyne/cm; (18)Density: 0.847 g/cm3; (19)Flash Point: 134.9 °C; (20)Enthalpy of Vaporization: 63.74 kJ/mol; (21)Boiling Point: 309 °C at 760 mmHg; (22)Vapour Pressure: 5.97E-05 mmHg at 25°C.
Production method of this chemical: The 11-Hexadecen-1-ol, (11E)- could be obtained by the reactants of (11-Hydroxyundecyl)-triphenylphosphoniumbromid and pentanal. This reaction needs the reagent of DMSO, NaH, and the solvent of tetrahydrofuran. The yield is 63 %. In addition, this reaction should be taken for 30 minutes.
Uses of this chemical: The 11-Hexadecen-1-ol, (11E)- could react with acetic acid anhydride, and obtain the 11-hexadecenyl acetate. This reaction needs the reagent of pyridine. The yield is 100 %.
You can still convert the following datas into molecular structure:
1.SMILES: OCCCCCCCCCC/C=C/CCCC
2.InChI: InChI=1/C16H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h5-6,17H,2-4,7-16H2,1H3/b6-5+
3.InChIKey: RHVMNRHQWXIJIS-AATRIKPKBB