Skip to Content
Merck
All Photos(1)

Key Documents

253871

Sigma-Aldrich

1-Nonyne

99%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3(CH2)6C≡CH
CAS Number:
Molecular Weight:
124.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

16 mmHg ( 37.7 °C)

Assay

99%

form

liquid

refractive index

n20/D 1.422 (lit.)

bp

150-151 °C (lit.)

mp

−50 °C (lit.)

density

0.757 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCC#C

InChI

1S/C9H16/c1-3-5-7-9-8-6-4-2/h1H,4-9H2,2H3

InChI key

OSSQSXOTMIGBCF-UHFFFAOYSA-N

General description

1-Nonyne reacts with thianthrene cation radical tetrafluoroborate to form trans-1,2-bis(5-thianthreniumyl)alkene tetrafluoroborate.

Application

1-Nonyne has been used in enantioselective synthesis of cladospolide B, C and (ent)-cladospolide D.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

93.2 °F - closed cup

Flash Point(C)

34 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Paramashivappa Rangappa et al.
The Journal of organic chemistry, 70(24), 9764-9770 (2005-11-19)
[structure: see text] Thianthrene cation radical tetrafluoroborate (Th*+ BF4(-)) added to the terminal alkynes 1-pentyne, 1-hexyne, 1-heptyne, 1-octyne, 1-nonyne, and 1-decyne to form trans-1,2-bis(5-thianthreniumyl)alkene tetrafluoroborates (1-6). Similarly, addition of phenoxathiin cation radical tetrafluoroborate (PO*+ BF4(-)) to the same alkynes gave
Yalan Xing et al.
Organic letters, 11(5), 1107-1110 (2009-02-06)
The enantioselective synthesis of cladospolide B, C, and (ent)-cladospolide D has been achieved in 11-15 steps from 1-nonyne. The route relies upon an alkyne zipper reaction to relay an ynone and dienoate functional groups across a nine carbon fragment, which

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service