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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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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' versatility enables reactions like addition, metathesis, hydroboration, cleavage, coupling, and cycloadditions in synthetic chemistry.

Alkynes' versatility enables reactions like addition, metathesis, hydroboration, cleavage, coupling, and cycloadditions in synthetic chemistry.

Alkynes' versatility enables reactions like addition, metathesis, hydroboration, cleavage, coupling, and cycloadditions in synthetic chemistry.

Alkynes' versatility enables reactions like addition, metathesis, hydroboration, cleavage, coupling, and cycloadditions in synthetic chemistry.

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