3-Bromopropoxy t-Butyl-Dimethylsilane

Names

[ Name ]:
3-Bromopropoxy t-Butyl-Dimethylsilane

[Synonym ]:
3-bromopropoxy-tert-butyl-dimethylsilane
(3-Bromopropoxy)(tert-butyl)dimethylsilane
Silane, (3-bromopropoxy)(1,1-dimethylethyl)dimethyl-
MFCD00216589
Propane, 1-bromo-3-(t-butyldimethylsilyloxy)-
(3-Bromopropoxy)(dimethyl)(2-methyl-2-propanyl)silane
3-Bromopropoxy t-Butyl-Dimethylsilane

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
219.2±23.0 °C at 760 mmHg

[ Molecular Formula ]:
C₉H₂₁BrOSi

[ Molecular Weight ]:
253.252

[ Flash Point ]:
86.4±22.6 °C

[ Exact Mass ]:
252.054489

[ PSA ]:
9.23000

[ LogP ]:
4.14

[ Vapour Pressure ]:
0.2±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.445

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
26

[ WGK Germany ]:
3

[ HS Code ]:
2931900090

Synthetic Route

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Precursor & DownStream

Precursor

DownStream

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

Synthesis and selective cyclooxygenase-2 inhibitory activity of a series of novel, nitric oxide donor-containing pyrazoles.

J. Med. Chem. 47 , 2180-2193, (2004)

The synthesis of a series of novel pyrazoles containing a nitrate (ONO(2)) moiety as a nitric oxide (NO)-donor functionality is reported. Their COX-1 and COX-2 inhibitory activities in human whole blo...

A concise total synthesis of (+/-)-vigulariol.

Angew. Chem. Int. Ed. Engl. 46 , 437, (2007)

Synthetic approaches to indolo[6,7-a]pyrrolo[3,4-c]carbazoles: potent cyclin D1/CDK4 inhibitors.

J. Org. Chem. 69 , 2967-2975, (2004)

Synthesis of indolo[6,7-a]pyrrolo[3,4-c]carbazoles 1, a new class of cyclin D1/CDK4 inhibitors, by oxidation of the corresponding aryl indolylmaleimides 2, will be described. Two approaches to the syn...