Bis(trimethylsilyl)acetylene


  • CasNo 14630-40-1
  • Purity 99%
Inquery

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1.What is the Bis(trimethylsilyl)acetylene ?

BTMSA is used as starting reagent in the synthesis of functionalized 4-R-1,2-bis(trimethylsilyl)benzenes. It is also used in the synthesis of (+)-brasilenyne2 and (β-diketanato)Ag(BTMSA). Bis(trimethylsilyl)acetylene is a ligand that binds to a central metal ion (e.g. Titanium) to create a coordination complex. One of its complexes, Permethyltitanocene-bis(trimethylsilyl)acetylene, is a catalyst for the head-to-tail dimerization of 1-alkynes (e.g. 3-Penten-1-yne [P227430]).

N,N'-bis(trimethylsilyl)sulfurdiimide
503027-47-2,503027-48-3,155139-78-9,18156-25-7

N,N'-bis(trimethylsilyl)sulfurdiimide

(C5Me5)2Ti(η(2)-bis(trimethylsilyl)acetylene)
128541-33-3

(C5Me5)2Ti(η(2)-bis(trimethylsilyl)acetylene)

bis(η5-pentamethylcyclopentadienyl)(trisulfido)titanium(IV)

bis(η5-pentamethylcyclopentadienyl)(trisulfido)titanium(IV)

[Ti(NHSi(CH<sub>3</sub>)3)(S(NSi(CH<sub>3</sub>)3)3)(C<sub>5</sub>(CH<sub>3</sub>)5)]
1416042-53-9

[Ti(NHSi(CH3 )3)(S(NSi(CH3 )3)3)(C5 (CH3 )5)]

[Ti<sub>2</sub>(NHSi(CH<sub>3</sub>)3)2(N(Si(CH<sub>3</sub>)3)SS)2(C<sub>5</sub>(CH<sub>3</sub>)5)2]
1416042-52-8

[Ti2 (NHSi(CH3 )3)2(N(Si(CH3 )3)SS)2(C5 (CH3 )5)2]

1,2,3,4-tetramethylfulvene
76089-59-3

1,2,3,4-tetramethylfulvene

Bis(trimethylsilyl)ethyne
14630-40-1

Bis(trimethylsilyl)ethyne

Conditions
Conditions Yield
In hexane; under Ar, Ti complex (0.706 mmol) dissolved in hexane (10 ml), N,N-bis(trimethylsilyl)sulfurdiimide added, mixt. stirred at 50°C for 5 d; amount of solvent reduced at 0°C, distilled at 70°C and 0.1 mbar to reveal 1,2,3,4-tetramethylfulvene, n-hexane, bis(trimethylsilyl)acetylene, and N,N'-bis(trimethylsilyl)sulfurdiimide, solid dissolved in n-hexane, stored at -78°C;
30%
8%
2%
Bis(trimethylsilyl)thioketene
62827-97-8

Bis(trimethylsilyl)thioketene

trimethyl(prop-1-ynyl)silane
6224-91-5

trimethyl(prop-1-ynyl)silane

tetramethylcyclodisilthiane
7796-59-0

tetramethylcyclodisilthiane

Trimethylsilanyl-ethenethione

Trimethylsilanyl-ethenethione

Bis(trimethylsilyl)ethyne
14630-40-1

Bis(trimethylsilyl)ethyne

Conditions
Conditions Yield
at 768 ℃; flash vacuum pyrolysis;
17 % Chromat.
17 % Chromat.
4 % Chromat.
13 % Chromat.

2.What is the CAS number for Bis(trimethylsilyl)acetylene ?

The CAS number of Bis(trimethylsilyl)acetylene is 14630-40-1.

More information of Bis(trimethylsilyl)acetylene 14630-40-1 are:

CAS?Number

14630-40-1

Density

0.791 g/cm3

Melting Point

21-24 °C

Boiling Point

134.6 °C at 760 mmHg

Flash Point

17.1 °C

Vapor Pressure

9.9mmHg at 25°C

Refractive Index

n20/D 1.427(lit.)

HS CODE

29310095

3.What are another words for Bis(trimethylsilyl)acetylene ?

Synonyms?for?Bis(trimethylsilyl)acetylene 14630-40-1:2,5-Disilahex-3-yne,2,2,5,5-tetramethyl- (6CI,7CI,8CI);Silane, 1,2-ethynediylbis[trimethyl- (9CI);1,2-Bis(trimethylsilanyl)ethyne;1,2-Bis(trimethylsilyl)ethyne;Bis(trimethylsilyl)ethyne;

4.What is the molecular formula of Bis(trimethylsilyl)acetylene?

The chemical formula of ?Bis(trimethylsilyl)acetylene is?C8H18Si2 which containing 8 Carbon atoms,18 Hydrogen atoms and 2 Silicon atoms,and the molecular weight of??Bis(trimethylsilyl)acetylene?is 170.402.

5.What is Bis(trimethylsilyl)acetylene (14630-40-1) used for?

Bis(trimethylsilyl)acetylene, also known as BTMSA, is a versatile chemical compound that participates as a nucleophile in Friedel-Crafts type acylations and alkylations. It is characterized by a center of inversion present on its triple bond and is a clear colorless liquid after melting. BTMSA is used as a starting reagent in the synthesis of various organic compounds and as a ligand in coordination complexes.

InChI:InChI=1/C8H18Si2/c1-9(2,3)7-8-10(4,5)6/h1-6H3

Relevant articles related to Bis(trimethylsilyl)acetylene:

Article

Source

REACTION OF GERMYLENE WITH THIOKETENES: SYNTHESIS OF ALKYLIDENEDIGERMATHIETANES

Ando, Wataru,Tsumuraya, Takeshi,Goto, Midori

, p. 5105 - 5108 (1986)

Phosphinidene Reactivity of a Transient Vanadium P≡N Complex

Courtemanche, Marc-André,Transue, Wesley J.,Cummins, Christopher C.

, p. 16220 - 16223 (2016)

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