Cas 86967-39-7,2-(Bis-methylsulfanyl-methylene)-3-[2-(4-methoxy-phenyl)-2-oxo-eth-(E)-ylidene]-succinic acid dimethyl ester

86967-39-7

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Basic information

Product Name: 2-(Bis-methylsulfanyl-methylene)-3-[2-(4-methoxy-phenyl)-2-oxo-eth-(E)-ylidene]-succinic acid dimethyl ester
Synonyms:
CAS NO:86967-39-7
Molecular Formula:
Molecular Weight: 396.485
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-(Bis-methylsulfanyl-methylene)-3-[2-(4-methoxy-phenyl)-2-oxo-eth-(E)-ylidene]-succinic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(Bis-methylsulfanyl-methylene)-3-[2-(4-methoxy-phenyl)-2-oxo-eth-(E)-ylidene]-succinic acid dimethyl ester(86967-39-7)
EPA Substance Registry System: 2-(Bis-methylsulfanyl-methylene)-3-[2-(4-methoxy-phenyl)-2-oxo-eth-(E)-ylidene]-succinic acid dimethyl ester(86967-39-7)

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: 86967-39-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86967-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,6 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86967-39:
(7*8)+(6*6)+(5*9)+(4*6)+(3*7)+(2*3)+(1*9)=197
197 % 10 = 7
So 86967-39-7 is a valid CAS Registry Number.

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86967-39-7Relevant academic research and scientific papers

Keten Dithioacetals. Part 22. Reaction of Polarised Ketoketen Dithioacetals with Dimethyl Acetylenedicarboxylate

Vishwakarma, Jai N.,Ila, Hiriyakkanavar,Junjappa, Hiriyakkanavar

, p. 1099 - 1102 (2007/10/02)

Ketoketen dithioacetals (1a-e) react with dimethyl acetylenedicarboxylate (2) to give open-chain dienes (4a-e) respectively.The formation of these dienes is explained through ring opening of the cyclobutene formed by cycloadditions of (1) and (2).The

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