Cas 1140919-91-0,(R,2E)-ethyl4-((2R,6S)-6-ethoxy-5,6-dihydro-2H-pyran-2-yl)-4-triisopropylsilyloxy-3-methylbut-2-enoate

1140919-91-0

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Basic information

Product Name: (R,2E)-ethyl4-((2R,6S)-6-ethoxy-5,6-dihydro-2H-pyran-2-yl)-4-triisopropylsilyloxy-3-methylbut-2-enoate
Synonyms: (R,2E)-ethyl4-((2R,6S)-6-ethoxy-5,6-dihydro-2H-pyran-2-yl)-4-triisopropylsilyloxy-3-methylbut-2-enoate
CAS NO:1140919-91-0
Molecular Formula:
Molecular Weight: 426.669
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: (R,2E)-ethyl4-((2R,6S)-6-ethoxy-5,6-dihydro-2H-pyran-2-yl)-4-triisopropylsilyloxy-3-methylbut-2-enoate(CAS DataBase Reference)
NIST Chemistry Reference: (R,2E)-ethyl4-((2R,6S)-6-ethoxy-5,6-dihydro-2H-pyran-2-yl)-4-triisopropylsilyloxy-3-methylbut-2-enoate(1140919-91-0)
EPA Substance Registry System: (R,2E)-ethyl4-((2R,6S)-6-ethoxy-5,6-dihydro-2H-pyran-2-yl)-4-triisopropylsilyloxy-3-methylbut-2-enoate(1140919-91-0)

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: 1140919-91-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1140919-91-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,0,9,1 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1140919-91:
(9*1)+(8*1)+(7*4)+(6*0)+(5*9)+(4*1)+(3*9)+(2*9)+(1*1)=140
140 % 10 = 0
So 1140919-91-0 is a valid CAS Registry Number.

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1140919-91-0Relevant academic research and scientific papers

Synthesis and preliminary antibacterial evaluation of simplified thiomarinol analogs

Marion, Olivier,Gao, Xuri,Marcus, Sandra,Hall, Dennis G.

, p. 1006 - 1017 (2009)

A series of simplified thiomarinol derivatives was prepared by way of catalytic enantioselective inverse electron demand hetero [4 + 2] cycloaddition/allylboration tandem reaction. As a preliminary evaluation, these analogs were tested for antimicrobial a

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