Cas 851341-17-8,acetic acid (2E,6E,10E)-12-(4-formyloxy-2-methoxy-phenoxy)-3,7,11-trimethyl-dodeca-2,6,10-trienyl ester

851341-17-8

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Basic information

Product Name: acetic acid (2E,6E,10E)-12-(4-formyloxy-2-methoxy-phenoxy)-3,7,11-trimethyl-dodeca-2,6,10-trienyl ester
Synonyms: acetic acid (2E,6E,10E)-12-(4-formyloxy-2-methoxy-phenoxy)-3,7,11-trimethyl-dodeca-2,6,10-trienyl ester
CAS NO:851341-17-8
Molecular Formula:
Molecular Weight: 430.541
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: acetic acid (2E,6E,10E)-12-(4-formyloxy-2-methoxy-phenoxy)-3,7,11-trimethyl-dodeca-2,6,10-trienyl ester(CAS DataBase Reference)
NIST Chemistry Reference: acetic acid (2E,6E,10E)-12-(4-formyloxy-2-methoxy-phenoxy)-3,7,11-trimethyl-dodeca-2,6,10-trienyl ester(851341-17-8)
EPA Substance Registry System: acetic acid (2E,6E,10E)-12-(4-formyloxy-2-methoxy-phenoxy)-3,7,11-trimethyl-dodeca-2,6,10-trienyl ester(851341-17-8)

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: 851341-17-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 851341-17-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,3,4 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 851341-17:
(8*8)+(7*5)+(6*1)+(5*3)+(4*4)+(3*1)+(2*1)+(1*7)=148
148 % 10 = 8
So 851341-17-8 is a valid CAS Registry Number.

851341-17-8Upstream product

4128-17-0 (2E,6E)-farnesyl acetate

851341-17-8Downstream Products

945609-15-4 4-[(2E,6E,10E)-12-hydroxy-2,6,10-trimethyl-dodeca-2,6,10-trienyloxy]-3-methoxy-phenol

851341-17-8Relevant academic research and scientific papers

Concise synthesis of (±)-smenochromene D (= likonide B)

Olson, Brooke S.,Trauner, Dirk

, p. 700 - 702 (2005)

The total synthesis of smenochromene D, an unusual ansa-terpenoid is described. The synthesis features an unprecedented macrocyclization proceeding through a biomimetic electrocyclization. The enantiomeric relationship between smenochromene D and likonide

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