产品名称
(S)-(+)-2-庚醇, 98%
InChI
1S/C7H16O/c1-3-4-5-6-7(2)8/h7-8H,3-6H2,1-2H3/t7-/m0/s1
SMILES string
CCCCC[C@H](C)O
InChI key
CETWDUZRCINIHU-ZETCQYMHSA-N
vapor density
4 (vs air)
vapor pressure
1 mmHg ( 15 °C)
assay
98%
form
liquid
optical activity
[α]24/D +10°, neat
optical purity
ee: 97% (GLC)
refractive index
n20/D 1.421 (lit.)
bp
149-150 °C (lit.)
density
0.815 g/mL at 25 °C (lit.)
functional group
hydroxyl
Quality Level
Application
(S)-(+)-2-Heptanol can be used as a starting material to synthesize:
- (S)-(+)-2-benzoyloxyheptane by treating with benzoyl anhydride and Et3N in the presence of DMAP.
- (S)-2-(p-toluenesulfonyl)heptane by reacting with p-toluenesulfonyl chloride.
- (+)-2-Heptyl acetate by treating with acetyl chloride.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
147.2 °F - closed cup
flash_point_c
64 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Enantioselective multidimensional gas chromatography of some secondary alcohols and their acetates from banana
Schubert, V, et al.
Zeitschrift fur Naturforschung B, 46(1-2), 33-36 (1991)
A study on the stereochemistry of direct conversion of polyamides to hydroxyesters using monomeric secondary chiral amines as a model compound
Kamimura A, et al.
Polymer Degradation and Stability, 160, 162-167 (2019)
Christiane Kiske et al.
Journal of agricultural and food chemistry, 64(45), 8563-8571 (2016-11-04)
The absolute configurations of chiral β-mercaptoalkanones were previously assigned on the basis of the 1H NMR anisotropy method using (S)-2-methoxy-2-(1-naphthyl)propionic acid ((S)-MαNP) as the chiral auxiliary. This study presents a reinvestigation of the configurations of 4-mercapto-2-pentanone 1, 4-mercapto-2-heptanone 2, and
商品
Chiral Alcohols
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