Cas 774593-63-4,(E)-2-[1-(4-Chloro-phenyl)-meth-(E)-ylidene]-4-methyl-hex-4-enoic acid methyl ester

774593-63-4

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Basic information

Product Name: (E)-2-[1-(4-Chloro-phenyl)-meth-(E)-ylidene]-4-methyl-hex-4-enoic acid methyl ester
Synonyms: (E)-2-[1-(4-Chloro-phenyl)-meth-(E)-ylidene]-4-methyl-hex-4-enoic acid methyl ester
CAS NO:774593-63-4
Molecular Formula:
Molecular Weight: 264.752
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: (E)-2-[1-(4-Chloro-phenyl)-meth-(E)-ylidene]-4-methyl-hex-4-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-2-[1-(4-Chloro-phenyl)-meth-(E)-ylidene]-4-methyl-hex-4-enoic acid methyl ester(774593-63-4)
EPA Substance Registry System: (E)-2-[1-(4-Chloro-phenyl)-meth-(E)-ylidene]-4-methyl-hex-4-enoic acid methyl ester(774593-63-4)

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: 774593-63-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 774593-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,4,5,9 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 774593-63:
(8*7)+(7*7)+(6*4)+(5*5)+(4*9)+(3*3)+(2*6)+(1*3)=214
214 % 10 = 4
So 774593-63-4 is a valid CAS Registry Number.

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774593-63-4Relevant academic research and scientific papers

Facile synthesis of lactones and dihydronaphthalenes from methyl 2-isobutenyl (or 2-isopentenyl)cinnamates as the common intermediates

Gowrisankar, Saravanan,Lee, Chang Gon,Kim, Jae Nyoung

, p. 6949 - 6953 (2007/10/03)

We prepared three different types of compounds, two α-alkylidene- γ-butyrolactones and 3,4-dihydronaphthalene-2-carboxylic acid from methyl 2-isobutenylcinnamates or methyl 2-isopentenylcinnamates as the common intermediates, which were derived from the acetates of Baylis-Hillman adducts.

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