Cas 124315-86-2,3,3-Bis-((E)-5-hydroxy-pent-2-enyl)-2-methyl-4-oxo-cyclohex-1-enecarboxylic acid ethyl ester

124315-86-2

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Basic information

Product Name: 3,3-Bis-((E)-5-hydroxy-pent-2-enyl)-2-methyl-4-oxo-cyclohex-1-enecarboxylic acid ethyl ester
Synonyms: 3,3-Bis-((E)-5-hydroxy-pent-2-enyl)-2-methyl-4-oxo-cyclohex-1-enecarboxylic acid ethyl ester
CAS NO:124315-86-2
Molecular Formula:
Molecular Weight: 350.455
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: 3,3-Bis-((E)-5-hydroxy-pent-2-enyl)-2-methyl-4-oxo-cyclohex-1-enecarboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3,3-Bis-((E)-5-hydroxy-pent-2-enyl)-2-methyl-4-oxo-cyclohex-1-enecarboxylic acid ethyl ester(124315-86-2)
EPA Substance Registry System: 3,3-Bis-((E)-5-hydroxy-pent-2-enyl)-2-methyl-4-oxo-cyclohex-1-enecarboxylic acid ethyl ester(124315-86-2)

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: 124315-86-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124315-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,1 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 124315-86:
(8*1)+(7*2)+(6*4)+(5*3)+(4*1)+(3*5)+(2*8)+(1*6)=102
102 % 10 = 2
So 124315-86-2 is a valid CAS Registry Number.

124315-86-2Upstream product

124315-86-2Downstream Products

124315-86-2Relevant academic research and scientific papers

HIGHLY STEREOSELECTIVE SYNTHESIS OF DI- AND TRISUBSTITUTED HOMOALLYLIC ALCOHOLS VIA PALLADIUM(O)-CATALYZED NUCLEOPHILIC OPENING OF VINYLIC OXETANES

Larock, Richard C.,Stolz-Dunn, Sandra K.

, p. 3487 - 3490 (2007/10/02)

Vinylic oxetanes react in an SN2' manner with a variety of potential nucleophiles in the presence of catalytic amounts of Pd(PPh3)4 to afford the corresponding highly functionalized, di- and trisubstituted homoallylic alcohols with high stereos

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