545449
5-Decyne
98%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
CH3(CH2)3C≡C(CH2)3CH3
CAS Number:
Molecular Weight:
138.25
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
5-Decyne, 98%
InChI
1S/C10H18/c1-3-5-7-9-10-8-6-4-2/h3-8H2,1-2H3
SMILES string
CCCCC#CCCCC
InChI key
JWBQJUFCNOLNNC-UHFFFAOYSA-N
assay
98%
refractive index
n20/D 1.4340 (lit.)
density
0.766 g/mL at 25 °C (lit.)
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
5-Decyne may be used in the preparation of:
- B
- -(cis-5-decenyl)-9-BBN (9-BBN= 9-borabicyclo[3,3,1]nonane)
- 5-decanone
- (Z)-5-ethyl-6-decene
- trans-5-decene
General description
5-Decyne is a symmetrical dialkylacetylene derivative that can be prepared from 1-hexyne.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
136.4 °F - closed cup
flash_point_c
58 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Regulatory Information
危险化学品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Hydroboration. 50. Hydroboration of representative alkynes with 9-borabicyclo [3.3.1] nonane-a simple synthesis of versatile vinyl bora and gem-dibora intermediates.
Brown HC, et al.
Journal of the American Chemical Society, 101(1), 96-99 (1979)
Reduction of organic compounds by lithium in low molecular weight amines. II. Stereochemistry. Chemical reduction of an isolated non-terminal double bond.
Benkeser RA, et al.
Journal of the American Chemical Society, 77(12), 3378-3379 (1955)
Highly selective and practical alkyne-alkyne cross-coupling using Cp2ZrBu2 and ethylene.
Xi Z, et al.
The Journal of Organic Chemistry, 60(14), 4444-4448 (1995)
Structure-activity relationships in the destruction of cytochrome P-450 mediated by certain ethynyl-substituted compounds in rats.
I N White
Biochemical pharmacology, 29(24), 3253-3255 (1980-12-01)
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