2627-95-4|Divinyltetramethyldisiloxane - Shanghai Canbi Pharma Ltd.

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Divinyltetramethyldisiloxane | CAS:2627-95-4

Divinyltetramethyldisiloxane

Name：Divinyltetramethyldisiloxane
CAS：2627-95-4
Synonyms：1,1,3,3-Tetramethyl-1,3-divinyldisiloxane; 1,3-Diethenyl-1,1,3,3-tetramethyl-disiloxane; 1,3-Divinyltetramethyldisiloxane
Molecular Formula：C₈H₁₈OSi₂
Molecular Weight：186.40
EINESC：220-099-6

Description

Properties

Melting point	-99.7 ºC
Water Solubility	Insoluble
Boiling point	139 ºC
Flash point	24 ºC
Density	0.813
Refractive index	1.411-1.413

Safety

Symbol(GHS)	F;Xi
Hazard Codes	R10;R36/37/38
SDS/MSDS	S16;S26;S37/39

SDS

Source	SDS/MSDS Samples
Alfa-Aesar	View & Download
Sigma-Aldrich	View & Download
TCI	View & Download

Synthetic Route

Name	CAS

Articles

Peer-Reviewed Papers

An expedient and multikilogram synthesis of a naphthalenoid H3 antagonist.Pu YM, et al. Organic Process Research & Development, 11(6), 1004-1009 (2007) Structure?activity relationships of arylbenzofuran H 3 receptor antagonistsGfesser, Gregory A., et al. Bioorganic & Medicinal Chemistry Letters, 15.10, 2559-2563 (2005) Optical Activation of Racemic a-Substituted Carbonyl Compounds Using Optically Active Amines.Matsushita H, et al. Bulletin of the Chemical Society of Japan, 49(7), 1928-1930 (1976) In vitro SAR of pyrrolidine-containing histamine H 3 receptor antagonists: Trends across multiple chemical seriesNersesian, Diana L., et al. Bioorganic & Medicinal Chemistry Letters, 18.1, 355-359 (2008) Synthesis and structure?activity relationships of 4, 5-fused pyridazinones as histamine H 3 receptor antagonistsTao, Ming, et al. Bioorganic & Medicinal Chemistry Letters, 21.20, 6126-6130 (2011) A new class of potent non-imidazole H 3 antagonists: 2-aminoethylbenzofuransCowart, Marlon, et al. Bioorganic & Medicinal Chemistry Letters, 14.3, 689-693 (2004) Synthesis and evaluation of pyridazinone?phenethylamine derivatives as selective and orally bioavailable histamine H 3 receptor antagonists with robust wake-promoting activityreddy Dandu, Reddeppa, et al. Bioorganic & Medicinal Chemistry Letters, 21.21, 6362-6365 (2011) Identification of pyridazin-3-one derivatives as potent, selective histamine H 3 receptor inverse agonists with robust wake activityHudkins, Robert L., et al. Bioorganic & Medicinal Chemistry Letters, 21.18, 5493-5497 (2011) Organic Process Research & Development, 11, 1004-1004 (2007)

Remarks

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Name	CAS

Description

Properties

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SDS

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