Cas 200124-85-2,[(E)-4-Benzyloxy-2-methyl-1-(3-methyl-1,1-dioxo-2,5-dihydro-1H-1λ<sup>6</sup>-thiophen-2-yl)-but-2-enyloxy]-trimethyl-silane

200124-85-2

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Basic information

Product Name: [(E)-4-Benzyloxy-2-methyl-1-(3-methyl-1,1-dioxo-2,5-dihydro-1H-1λ⁶-thiophen-2-yl)-but-2-enyloxy]-trimethyl-silane
Synonyms:
CAS NO:200124-85-2
Molecular Formula:
Molecular Weight: 394.607
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: [(E)-4-Benzyloxy-2-methyl-1-(3-methyl-1,1-dioxo-2,5-dihydro-1H-1λ⁶-thiophen-2-yl)-but-2-enyloxy]-trimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: [(E)-4-Benzyloxy-2-methyl-1-(3-methyl-1,1-dioxo-2,5-dihydro-1H-1λ⁶-thiophen-2-yl)-but-2-enyloxy]-trimethyl-silane(200124-85-2)
EPA Substance Registry System: [(E)-4-Benzyloxy-2-methyl-1-(3-methyl-1,1-dioxo-2,5-dihydro-1H-1λ⁶-thiophen-2-yl)-but-2-enyloxy]-trimethyl-silane(200124-85-2)

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: 200124-85-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 200124-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,0,1,2 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 200124-85:
(8*2)+(7*0)+(6*0)+(5*1)+(4*2)+(3*4)+(2*8)+(1*5)=62
62 % 10 = 2
So 200124-85-2 is a valid CAS Registry Number.

200124-85-2Upstream product

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200124-85-2Relevant academic research and scientific papers

Convenient synthesis of 1,3,6-triene systems through alkylation of 3-methyl-3-sulfolene

Subramanian,Padmakumar,Bhat, Sujata V.

, p. 4067 - 4072 (2007/10/03)

Various 1,3,6-triene systems have been synthesised through alkylation of 3-methyl-3-sulfolene with conjugated aldehydes followed by silylation and subsequent desulfonylation. A new route to synthesis of (+/-)-α-chamigrene, isofokienol and 5-hydroxy-α-farn

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