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541672

Sigma-Aldrich

4-(tert-Butyldimethylsilyloxy)-1-butyne

97%

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About This Item

Linear Formula:
CH≡C(CH2)2OSi(CH3)2C(CH3)3
CAS Number:
Molecular Weight:
184.35
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

refractive index

n20/D 1.43 (lit.)

bp

70-74 °C/10 mmHg (lit.)

density

0.893 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)[Si](C)(C)OCCC#C

InChI

1S/C10H20OSi/c1-7-8-9-11-12(5,6)10(2,3)4/h1H,8-9H2,2-6H3

InChI key

NUZBJLXXTAOBPH-UHFFFAOYSA-N

Application

4-(tert-Butyldimethylsilyloxy)-1-butyne may be used in the synthesis of 1-(tert-butyldimethylsilyloxy)-3-pentyn-5-ol and 1-(tert-butyldimethylsilyloxy)-6,6-dimethyl-3-heptyn-5-ol.

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)

136.9 °F - closed cup

Flash Point(C)

58.3 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Dihydrofurans via an Intramolecular Alkoxide Addition to an Allenylphosphine Oxide.
Pravia K, et al.
The Journal of Organic Chemistry, 61(17), 6031-6032 (1996)

Articles

Alkynes contain a highly versatile functional group that may be utilized for numerous reactions such as electrophilic additions of hydrogen, halogens, hydrogen halides, or water; metathesis; hydroboration; oxidative cleavage; C–C coupling; and cycloadditions

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