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(2-Bromoethoxy)-Tert-Butyldimethylsilane

Names

[ CAS No. ]:
86864-60-0

[ Name ]:
(2-Bromoethoxy)-Tert-Butyldimethylsilane

[Synonym ]:
2-Bromoethoxy-tert-butyldimethylsilane
(2-Bromoethoxy)(tert-butyl)dimethylsilane
(2-Bromoethoxy)(dimethyl)(2-methyl-2-propanyl)silane
2-bromoethoxy-tert-butyl-dimethylsilane
Silane, (2-bromoethoxy)(1,1-dimethylethyl)dimethyl-
MFCD00209550
(2-Bromoethoxy)-t-Butyl-Dimethylsilane
(2-Bromoethoxy)dimethyl-tert-butylsilane

Chemical & Physical Properties

[ Density]:
1.107

[ Boiling Point ]:
191 ºC

[ Molecular Formula ]:
C8H19BrOSi

[ Molecular Weight ]:
239.225

[ Flash Point ]:
69 ºC

[ Exact Mass ]:
238.038849

[ PSA ]:
9.23000

[ LogP ]:
3.83

[ Appearance of Characters ]:
Liquid | White to pale yellow

[ Vapour Pressure ]:
0.7±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.443

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P305 + P351 + P338

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
26-36

[ WGK Germany ]:
3

[ HS Code ]:
2931900090

Synthetic Route

Customs

[ HS Code ]: 2931900090

[ Summary ]:
2931900090. other organo-inorganic compounds. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:6.5%. General tariff:30.0%

Articles

Structure-activity relationship study of N⁶-(2-(4-(1H-Indol-5-yl)piperazin-1-yl)ethyl)-N⁶-propyl-4,5,6,7-tetrahydrobenzo[d]thiazole-2,6-diamine analogues: development of highly selective D3 dopamine receptor agonists along with a highly potent D2/D3 agonist and their pharmacological characterization.

J. Med. Chem. 55(12) , 5826-40, (2012)

In our effort to develop multifunctional drugs against Parkinson's disease, a structure-activity-relationship study was carried out based on our hybrid molecular template targeting D2/D3 receptors. Co...

A route to annulated indoles via a palladium-catalyzed tandem alkylation/direct arylation reaction.

J. Am. Chem. Soc. 127(38) , 13148-13149, (2005)

A norbornene-mediated palladium-catalyzed tandem alkylation/C-H functionalization sequence is described, in which an alkyl-aryl bond and a heteroaryl-aryl bond are formed in one pot. A variety of high...

Hansen, Joshua; et al.

Tetrahedron Lett. 47(1) , 69-72, (2005)


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