Cas 136367-87-8,1,2-bis(1-phenyl-3-butenoxy)ethane

136367-87-8

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Basic information

Product Name: 1,2-bis(1-phenyl-3-butenoxy)ethane
Synonyms: 1,2-bis(1-phenyl-3-butenoxy)ethane
CAS NO:136367-87-8
Molecular Formula:
Molecular Weight: 322.447
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: 1,2-bis(1-phenyl-3-butenoxy)ethane(CAS DataBase Reference)
NIST Chemistry Reference: 1,2-bis(1-phenyl-3-butenoxy)ethane(136367-87-8)
EPA Substance Registry System: 1,2-bis(1-phenyl-3-butenoxy)ethane(136367-87-8)

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: 136367-87-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 136367-87-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,3,6 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 136367-87:
(8*1)+(7*3)+(6*6)+(5*3)+(4*6)+(3*7)+(2*8)+(1*7)=148
148 % 10 = 8
So 136367-87-8 is a valid CAS Registry Number.

136367-87-8Upstream product

136367-87-8Downstream Products

136367-87-8Relevant academic research and scientific papers

Catalytic ring-opening allylation of cyclic acetals with allylsilanes using silica-alumina

Motokura, Ken,Yoneda, Hirokazu,Miyaji, Akimitsu,Baba, Toshihide

supporting information; experimental part, p. 1373 - 1375 (2010/09/08)

Ring-opening allylation of cyclic acetals has required stoichiometric amounts of Lewis acids. In this paper, catalytic ring-opening allylation in the presence of silica-alumina is reported. This ring-opening allylation showed high atom economy. Consecutiv

"Cation pool" method based on C-C bond dissociation. Effective generation of monocations and dications

Okajima, Masayuki,Suga, Seiji,Itami, Kenichiro,Yoshida, Jun-Ichi

, p. 6930 - 6931 (2007/10/03)

The "cation pools" of alkoxyarylcarbenium ions were effectively generated by the oxidative C-C bond dissociation using low temperature electrolysis. The present method is especially effective for the generation and accumulation of dications, which react with carbon nucleophiles. Copyright

REACTIONS OF 1,3-DIOXACYCLOALKANES WITH TRIMETHYLPROPENYLSILANE

Mikhailova, I. Yu.,Mel'nitskii, I. A.,Kuladze, T. K.,Kantor, E. A.

, p. 710 - 713 (2007/10/02)

5-Oxa-8-trimethylsilyloxyoctenes are formed during the cleavage of 1,3-dioxacycloalkanes with trimethylpropenylsilane in the presence of metal halides.The use of boron trifluoride etherate changes the direction of the process and lead to the diallyl ether

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