Cas 28171-64-4,2,4-Pentadienoic acid, 3-methyl-5-(3,6,6-trimethyl-4-oxo-1-cyclohexen-1-yl)-, methyl ester, (E,E)-

28171-64-4

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Basic information

Product Name: 2,4-Pentadienoic acid, 3-methyl-5-(3,6,6-trimethyl-4-oxo-1-cyclohexen-1-yl)-, methyl ester, (E,E)-
Synonyms:
CAS NO:28171-64-4
Molecular Formula: C16H22O3
Molecular Weight: 262.349
EINECS: N/A
Product Categories: N/A
Mol File: 28171-64-4.mol
Article Data: 1

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: 2,4-Pentadienoic acid, 3-methyl-5-(3,6,6-trimethyl-4-oxo-1-cyclohexen-1-yl)-, methyl ester, (E,E)-(CAS DataBase Reference)
NIST Chemistry Reference: 2,4-Pentadienoic acid, 3-methyl-5-(3,6,6-trimethyl-4-oxo-1-cyclohexen-1-yl)-, methyl ester, (E,E)-(28171-64-4)
EPA Substance Registry System: 2,4-Pentadienoic acid, 3-methyl-5-(3,6,6-trimethyl-4-oxo-1-cyclohexen-1-yl)-, methyl ester, (E,E)-(28171-64-4)

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: 28171-64-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 28171-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,1,7 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 28171-64:
(7*2)+(6*8)+(5*1)+(4*7)+(3*1)+(2*6)+(1*4)=114
114 % 10 = 4
So 28171-64-4 is a valid CAS Registry Number.

28171-64-4Upstream product

28171-64-4Downstream Products

38962-47-9 methyl-(2E,4E)-3-methyl-5-(3'-hydroxy-2',6',6'-trimethylcyclohex-1'-en-1'-yl)-2,4-pentadienoate

28171-64-4Relevant articles and documents

Ionylideneacetic Acids and Abscisic Acid Biosynthesis by Cercospora rosicola

Norman, Shirley M.,Poling, Stephen M.,Maier, V. P.,Nelson, Mary D.

, p. 2317 - 2324 (2007/10/02)

Several compounds having the basic α-ionylideneacetic acid stucture were tested in Cercospora rosicola resuspensions.At 100 μM, all the compounds inhibited abscisic acid (ABA) biosynthesis.Time studies with unlabelled and deuterated (2Z,4E)- and (2E,4E)-α

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