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Carbamic acid, N-(6-hydroxyhexyl)-, 9H-fluoren-9-ylmethylester

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Name

Carbamic acid, N-(6-hydroxyhexyl)-, 9H-fluoren-9-ylmethylester

EINECS N/A
CAS No. 127903-20-2 Density 1.151 g/cm3
PSA 58.56000 LogP 4.46870
Solubility N/A Melting Point 119 °C
Formula C21H25NO3 Boiling Point 539.2 °C at 760 mmHg
Molecular Weight 339.434 Flash Point 279.9 °C
Transport Information N/A Appearance N/A
Safety Risk Codes N/A
Molecular Structure Molecular Structure of 127903-20-2 (6-(FMOC-AMINO)-1-HEXANOL) Hazard Symbols IrritantXi
Synonyms

6-(Fmoc-amino)-1-hexanol;

Article Data 13

Carbamic acid, N-(6-hydroxyhexyl)-, 9H-fluoren-9-ylmethylester Specification

The Carbamic acid, N-(6-hydroxyhexyl)-, 9H-fluoren-9-ylmethylester, with the CAS registry number of 127903-20-2, is also known as 6-(Fmoc-amino)-1-hexanol. Its molecular formula is C21H25NO3 and molecular weight is 339.43. What's more, its systematic name is 9H-Fluoren-9-ylmethyl (6-hydroxyhexyl)carbamate.

Physical properties about the Carbamic acid, N-(6-hydroxyhexyl)-, 9H-fluoren-9-ylmethylester are: (1)ACD/LogP: 4.21; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 4.21; (4)ACD/LogD (pH 7.4): 4.21; (5)ACD/BCF (pH 5.5): 930.88; (6)ACD/BCF (pH 7.4): 930.86; (7)ACD/KOC (pH 5.5): 4642.3; (8)ACD/KOC (pH 7.4): 4642.24; (9)#H bond acceptors: 4; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 10; (12)Polar Surface Area: 38.77 Å2; (13)Index of Refraction: 1.578; (14)Molar Refractivity: 97.82 cm3; (15)Molar Volume: 294.7 cm3; (16)Surface Tension: 48.7 dyne/cm; (17)Density: 1.151 g/cm3; (18)Flash Point: 279.9 °C; (19)Enthalpy of Vaporization: 85.93 kJ/mol; (20)Boiling Point: 539.2 °C at 760 mmHg; (21)Vapour Pressure: 1.86E-12 mmHg at 25 °C.

Preparation: this chemical is prepared by reaction of 6-Amino-hexan-1-ol with 9H-Fluoren-9-ylmethyl chloroformate. The reaction needs reagent Na2CO3 and solvent Acetone. The reaction time is 6 h. The yield is about 74 %.

The Carbamic acid, N-(6-hydroxyhexyl)-, 9H-fluoren-9-ylmethylester is used to produce 2-(9-Fluorenylmethoxycarbonyl)aminohexanol-(N,N-diisopropylmethyl)phosphonamidite

Uses: it is used to produce other chemicals. For example, it is used to produce 2-(9-Fluorenylmethoxycarbonyl)aminohexanol-(N,N-diisopropylmethyl)phosphonamidite. This reaction needs reagent N,N-Diisopropylethylamine. Meanwhile, it needs solvent CH2Cl2. The reaction time is 20 min. The yield is about 90 %.

The Carbamic acid, N-(6-hydroxyhexyl)-, 9H-fluoren-9-ylmethylester is used to produce 2-(9-Fluorenylmethoxycarbonyl)aminohexanol-(N,N-diisopropylmethyl)phosphonamidite

You can still convert the following datas into molecular structure:
(1) SMILES: O=C(OCC3c1ccccc1c2c3cccc2)NCCCCCCO
(2) InChI: InChI=1/C21H25NO3/c23-14-8-2-1-7-13-22-21(24)25-15-20-18-11-5-3-9-16(18)17-10-4-6-12-19(17)20/h3-6,9-12,20,23H,1-2,7-8,13-15H2,(H,22,24)
(3) InChIKey: VGXOJZUTHIGHPT-UHFFFAOYAI

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