<Suppliers Price>

(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)


More Articles


Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.