Cas 1236879-87-0,dimethyl [(2E,4E)-1-phenyl-3-(triisopropylsiloxy)hexa-2,4-dienyl](prop-2-ynyl)malonate

1236879-87-0

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Basic information

Product Name: dimethyl [(2E,4E)-1-phenyl-3-(triisopropylsiloxy)hexa-2,4-dienyl](prop-2-ynyl)malonate
Synonyms: dimethyl [(2E,4E)-1-phenyl-3-(triisopropylsiloxy)hexa-2,4-dienyl](prop-2-ynyl)malonate
CAS NO:1236879-87-0
Molecular Formula:
Molecular Weight: 498.735
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: dimethyl [(2E,4E)-1-phenyl-3-(triisopropylsiloxy)hexa-2,4-dienyl](prop-2-ynyl)malonate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl [(2E,4E)-1-phenyl-3-(triisopropylsiloxy)hexa-2,4-dienyl](prop-2-ynyl)malonate(1236879-87-0)
EPA Substance Registry System: dimethyl [(2E,4E)-1-phenyl-3-(triisopropylsiloxy)hexa-2,4-dienyl](prop-2-ynyl)malonate(1236879-87-0)

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: 1236879-87-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1236879-87-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,6,8,7 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1236879-87:
(9*1)+(8*2)+(7*3)+(6*6)+(5*8)+(4*7)+(3*9)+(2*8)+(1*7)=200
200 % 10 = 0
So 1236879-87-0 is a valid CAS Registry Number.

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1236879-87-0Relevant academic research and scientific papers

Gold-catalyzed tandem cyclization of dienol silyl ethers for the preparation of bicyclo[4.3.0]nonane derivatives

Kusama, Hiroyuki,Karibe, Yusuke,Onizawa, Yuji,Iwasawa, Nobuharu

, p. 4269 - 4272 (2010)

[Figure Presented] Tandem bicycle: A gold-catalyzed geminal carbo-functionalization reaction of 3-siloxy-1,3-dien-8-ynes proceeded smoothly to give bicyclo[4.3.0]nonanes stereoselectively through ring expansion of the bicyclic carbene complex intermediates. The product configuration was different from that of the thermal Diels-Alder adduct.

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