Cas 73003-76-6,2-Methyl-2-butenoic acid 2-methyl-2-butenyl ester

73003-76-6

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Basic information

Product Name: 2-Methyl-2-butenoic acid 2-methyl-2-butenyl ester
Synonyms: 2-Methyl-2-butenoic acid 2-methyl-2-butenyl ester;2-Butenoic acid, 2-methyl-, 2-methyl-2-buten-1-yl ester;2-Butenoic acid, 2-methyl-, 2-methyl-2-butenyl ester;2-Methyl-2-butenyl 2-methylcrotonate
CAS NO:73003-76-6
Molecular Formula: C10H16O2
Molecular Weight: 168.24
EINECS: N/A
Product Categories: N/A
Mol File: 73003-76-6.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-Methyl-2-butenoic acid 2-methyl-2-butenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Methyl-2-butenoic acid 2-methyl-2-butenyl ester(73003-76-6)
EPA Substance Registry System: 2-Methyl-2-butenoic acid 2-methyl-2-butenyl ester(73003-76-6)

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: 73003-76-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 73003-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,0,0 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73003-76:
(7*7)+(6*3)+(5*0)+(4*0)+(3*3)+(2*7)+(1*6)=96
96 % 10 = 6
So 73003-76-6 is a valid CAS Registry Number.

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73003-76-6Relevant academic research and scientific papers

Peroxides as plant constituents. 6. Hydroperoxides from the blossoms of Roman camomile, Anthemis nobilis L

Ruecker,Mayer,Lee

, p. 821 - 826 (1989)

From the ethanol extract of the blossoms of Anthemis nobilis L. (syn. Chamaemelum nobile L.), six new hydroperoxides (1-6) were isolated, besides the known 1 beta-hydroperoxyisonobilin (7). The structures were elucidated by spectroscopic methods and in some cases ascertained by synthesis. Compounds 2 and 3 show a medium antibacterial activity.

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