Cas 960010-30-4,(Z)-1,6-bis(trimethylsilyl)-3,4-bis(5'-phenyl-2'-methylthiophen-3'-yl)hex-3-ene-1,5-diyne

960010-30-4

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Basic information

Product Name: (Z)-1,6-bis(trimethylsilyl)-3,4-bis(5'-phenyl-2'-methylthiophen-3'-yl)hex-3-ene-1,5-diyne
Synonyms: (Z)-1,6-bis(trimethylsilyl)-3,4-bis(5'-phenyl-2'-methylthiophen-3'-yl)hex-3-ene-1,5-diyne
CAS NO:960010-30-4
Molecular Formula:
Molecular Weight: 564.963
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: (Z)-1,6-bis(trimethylsilyl)-3,4-bis(5'-phenyl-2'-methylthiophen-3'-yl)hex-3-ene-1,5-diyne(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-1,6-bis(trimethylsilyl)-3,4-bis(5'-phenyl-2'-methylthiophen-3'-yl)hex-3-ene-1,5-diyne(960010-30-4)
EPA Substance Registry System: (Z)-1,6-bis(trimethylsilyl)-3,4-bis(5'-phenyl-2'-methylthiophen-3'-yl)hex-3-ene-1,5-diyne(960010-30-4)

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: 960010-30-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 960010-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,0,1 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 960010-30:
(8*9)+(7*6)+(6*0)+(5*0)+(4*1)+(3*0)+(2*3)+(1*0)=124
124 % 10 = 4
So 960010-30-4 is a valid CAS Registry Number.

960010-30-4Upstream product

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960010-30-4Relevant academic research and scientific papers

Creating a reactive enediyne by using visible light: Photocontrol of the Bergman cyclization

Sud, David,Wigglesworth, Tony J.,Branda, Neil R.

, p. 8017 - 8019 (2008/09/18)

(Chemical Equation Presented) Visible changes: Visible light is used to create an active enediyne for Bergman cyclization by taking advantage of a well-known molecular photoswitch. Only isomer 2 has the enediyne structure required to produce a diradical that can be trapped as compound 3. Isomer 2 is formed from the thermally stable isomer 1 by stimulating the ring-opening reaction with visible light.

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