Cas 1430110-73-8,(E)-1,1-bis(ethoxymethyl)-3-(3-phenylallylidene)cyclobutane

1430110-73-8

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Basic information

Product Name: (E)-1,1-bis(ethoxymethyl)-3-(3-phenylallylidene)cyclobutane
Synonyms: (E)-1,1-bis(ethoxymethyl)-3-(3-phenylallylidene)cyclobutane
CAS NO:1430110-73-8
Molecular Formula:
Molecular Weight: 286.414
EINECS: N/A
Product Categories: N/A
Mol File: 1430110-73-8.mol
Article Data: 1

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)-1,1-bis(ethoxymethyl)-3-(3-phenylallylidene)cyclobutane(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1,1-bis(ethoxymethyl)-3-(3-phenylallylidene)cyclobutane(1430110-73-8)
EPA Substance Registry System: (E)-1,1-bis(ethoxymethyl)-3-(3-phenylallylidene)cyclobutane(1430110-73-8)

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: 1430110-73-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1430110-73-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,0,1,1 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1430110-73:
(9*1)+(8*4)+(7*3)+(6*0)+(5*1)+(4*1)+(3*0)+(2*7)+(1*3)=88
88 % 10 = 8
So 1430110-73-8 is a valid CAS Registry Number.

1430110-73-8Upstream product

16215-11-5 trans-cinnamyl p-tolyl sulfone

1430110-73-8Downstream Products

1430110-73-8Relevant articles and documents

Synthesis of small ring-containing conjugated dienes via the coupling reaction of cyclopropyl- and cyclobutylmagnesium carbenoids with α-sulfonylallyllithiums

Kimura, Tsutomu,Inumaru, Mio,Migimatsu, Takuma,Ishigaki, Masashi,Satoh, Tsuyoshi

, p. 3961 - 3970 (2013/06/27)

A variety of allylidenecyclopropanes and allylidenecyclobutanes were synthesized via the coupling reaction of cyclopropyl- and cyclobutylmagnesium carbenoids with α-sulfonylallyllithiums. Small ring cycloalkylmagnesium carbenoids were generated from aryl

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