Cas 943241-72-3,2-allyl-2-(6-hydroxy-6-phenyl-hexa-2,4-diynyl)-malonic acid diethyl ester

943241-72-3

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Basic information

Product Name: 2-allyl-2-(6-hydroxy-6-phenyl-hexa-2,4-diynyl)-malonic acid diethyl ester
Synonyms: 2-allyl-2-(6-hydroxy-6-phenyl-hexa-2,4-diynyl)-malonic acid diethyl ester
CAS NO:943241-72-3
Molecular Formula:
Molecular Weight: 368.43
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: 2-allyl-2-(6-hydroxy-6-phenyl-hexa-2,4-diynyl)-malonic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-allyl-2-(6-hydroxy-6-phenyl-hexa-2,4-diynyl)-malonic acid diethyl ester(943241-72-3)
EPA Substance Registry System: 2-allyl-2-(6-hydroxy-6-phenyl-hexa-2,4-diynyl)-malonic acid diethyl ester(943241-72-3)

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: 943241-72-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 943241-72-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,2,4 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 943241-72:
(8*9)+(7*4)+(6*3)+(5*2)+(4*4)+(3*1)+(2*7)+(1*2)=163
163 % 10 = 3
So 943241-72-3 is a valid CAS Registry Number.

943241-72-3Upstream product

943241-72-3Downstream Products

916462-22-1 2-(6-acetoxy-6-phenyl-hexa-2,4-diynyl)-2-allyl-malonic acid diethyl ester

943241-72-3Relevant academic research and scientific papers

Reactivity and selectivity of 1,3-diyn-6-enes in electrophilic transition metal-catalyzed reactions

Cho, Eun Jin,Kim, Mansuk,Lee, Daesung

, p. 5413 - 5416 (2006)

1,3-Diyne is an excellent source of alkynyl metal carbene species upon activation with an electrophilic metal catalyst. The products from this bond reorganization process suggest that the metal carbene species, generated from the preferential participatio

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