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340332

(S)-(+)-2-Heptanol

Name: (<I>S</I>)-(+)-2-Heptanol
Brand: ALDRICH

98%

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About This Item

Linear Formula:

CH₃(CH₂)₄CH(OH)CH₃

CAS Number:

6033-23-4

Molecular Weight:

116.20

NACRES:

NA.22

PubChem Substance ID:

24860798

UNSPSC Code:

12352001

MDL number:

MFCD00065003

Assay:

98%

Form:

liquid

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Properties

vapor density

4 (vs air)

Quality Level

100

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

SMILES string

CCCCC[C@H](C)O

InChI

1S/C7H16O/c1-3-4-5-6-7(2)8/h7-8H,3-6H2,1-2H3/t7-/m0/s1

InChI key

CETWDUZRCINIHU-ZETCQYMHSA-N

Description

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.

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

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

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Articles

Chiral Alcohols

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)

Reinvestigation of the Absolute Configurations of Chiral β-Mercaptoalkanones Using Vibrational Circular Dichroism and 1H NMR Analysis.

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

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)

Global Trade Item Number

SKU	GTIN
340332-1G	04061826753040