| Identification | More | [Name]
Bis(trimethylsilyl)acetylene | [CAS]
14630-40-1 | [Synonyms]
1,2-BIS-TRIMETHYLSILANYL-ETHYNE
BIS(TRIMETHYLSILYL)ACETYLENE
BSTMA
BTMSA
TIMTEC-BB SBB008997
1,2-Bis(trimethylsilyl)acetylene
1,2-Bis(trimethylsilyl)ethyne
1,2-ethynediylbis[trimethyl-silan
1,2-ethynediylbis[trimethyl-Silane
2,5-Disilahex-3-yne, 2,2,5,5-tetramethyl-
Acetylene, bis(trimethylsilyl)-
Bis(trimethylsilyl)ethyne
Silane, 1,2-ethynediylbis*trimethyl-
Trimethyl[(trimethylsilyl)ethynyl]silane
Bis(trimethylsilyl)acetylene(BTMSA)
Bis(trimethylsilyl)acetylene,min.97%
Ethynylbistrimethylsilanel
5-Fluoro-2-methoxy-phenylamine
Bis(trimethylsilyl)acetylene, min. 97% | [EINECS(EC#)]
238-671-9 | [Molecular Formula]
C8H18Si2 | [MDL Number]
MFCD00008276 | [Molecular Weight]
170.4 | [MOL File]
14630-40-1.mol |
| Safety Data | Back Directory | [Hazard Codes ]
F,Xi | [Risk Statements ]
R11:Highly Flammable.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S16:Keep away from sources of ignition-No smoking .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [RIDADR ]
UN 1993 3/PG 2
| [WGK Germany ]
3
| [F ]
10 | [TSCA ]
Yes | [HazardClass ]
3 | [PackingGroup ]
III | [HS Code ]
29310095 |
| Hazard Information | Back Directory | [Chemical Properties]
clear colorless liquid after melting | [Uses]
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]). | [Uses]
In the presence of CpCo(CO)2 (cat. no. 245259), undergoes cycloaddition with 1,5-hexadiynes to form benzocyclobutenes.1 | [General Description]
Bis(trimethylsilyl)acetylene (BTMSA) participates as nucleophile in Friedel-Crafts type acylations and alkylations. BTMSA undergoes rhodium catalyzed addition reaction with diarylacetylenes. It undergoes cycloaddition with 1,5-hexadiynes in the presence of CpCo(CO)2 (Cp=cyclopentadienyl) to form benzocyclobutenes. Structure of BTMSA was characterized by a centre of inversion present on triple bond (length=1.208(3)?). TiCl4-Et2AlCl catalyzed Diels-Alder reaction of BTMSA with norbornadiene has been reported. | [Purification Methods]
Dissolve it in pet ether and wash it with ice-cold dilute HCl. The pet ether extract is dried (MgSO4), evaporated and fractionated at 760mm. [Walton & Waugh J Organomet Chem 37 45 1972, Beilstein 4 IV 3950.] |
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