Cas 909282-22-0,<i>tert</i>-butyl-[2-(2,2-dimethyl-3-vinyl-cyclohex-3-enyloxy)-ethoxy]-dimethyl-silane

909282-22-0

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Basic information

Product Name: tert-butyl-[2-(2,2-dimethyl-3-vinyl-cyclohex-3-enyloxy)-ethoxy]-dimethyl-silane
Synonyms: tert-butyl-[2-(2,2-dimethyl-3-vinyl-cyclohex-3-enyloxy)-ethoxy]-dimethyl-silane
CAS NO:909282-22-0
Molecular Formula:
Molecular Weight: 310.552
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: tert-butyl-[2-(2,2-dimethyl-3-vinyl-cyclohex-3-enyloxy)-ethoxy]-dimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl-[2-(2,2-dimethyl-3-vinyl-cyclohex-3-enyloxy)-ethoxy]-dimethyl-silane(909282-22-0)
EPA Substance Registry System: tert-butyl-[2-(2,2-dimethyl-3-vinyl-cyclohex-3-enyloxy)-ethoxy]-dimethyl-silane(909282-22-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 909282-22-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 909282-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,2,8 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 909282-22:
(8*9)+(7*0)+(6*9)+(5*2)+(4*8)+(3*2)+(2*2)+(1*2)=180
180 % 10 = 0
So 909282-22-0 is a valid CAS Registry Number.

909282-22-0Upstream product

86864-60-0 2-(tert-butyldimethylsilyloxy)ethyl bromide

909282-22-0Downstream Products

909282-22-0Relevant academic research and scientific papers

Synthesis of novel chemical probes for the study of tanshinone binding proteins

Lee, Jin-Soo,Han, Sun-Young,Kim, Myong Sang,Yu, Chan-Mo,Kim, Myung Hee,Kim, Seong Hwan,Min, Yong Ki,Kim, Bum Tae

, p. 4733 - 4737 (2006)

Novel diazirine or biotin-labeled tanshinone probes were synthesized and evaluated for TRAP inhibitory activity against RANKL-induced osteoclastogenesis in RAW264.7 cells. We found that diazirine-labeled derivatives (18 and 20) are potent inhibitors of RA

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