Cas 1101200-64-9,(7Z,10Z,13Z,16Z,19Z)-1-(2,4,6-trimethoxyphenyl)docosa-7,10,13,16,19-pentaen-2-yn-1-ol

1101200-64-9

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Basic information

Product Name: (7Z,10Z,13Z,16Z,19Z)-1-(2,4,6-trimethoxyphenyl)docosa-7,10,13,16,19-pentaen-2-yn-1-ol
Synonyms: (7Z,10Z,13Z,16Z,19Z)-1-(2,4,6-trimethoxyphenyl)docosa-7,10,13,16,19-pentaen-2-yn-1-ol
CAS NO:1101200-64-9
Molecular Formula:
Molecular Weight: 478.672
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: (7Z,10Z,13Z,16Z,19Z)-1-(2,4,6-trimethoxyphenyl)docosa-7,10,13,16,19-pentaen-2-yn-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (7Z,10Z,13Z,16Z,19Z)-1-(2,4,6-trimethoxyphenyl)docosa-7,10,13,16,19-pentaen-2-yn-1-ol(1101200-64-9)
EPA Substance Registry System: (7Z,10Z,13Z,16Z,19Z)-1-(2,4,6-trimethoxyphenyl)docosa-7,10,13,16,19-pentaen-2-yn-1-ol(1101200-64-9)

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: 1101200-64-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1101200-64-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,1,2,0 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1101200-64:
(9*1)+(8*1)+(7*0)+(6*1)+(5*2)+(4*0)+(3*0)+(2*6)+(1*4)=49
49 % 10 = 9
So 1101200-64-9 is a valid CAS Registry Number.

1101200-64-9Upstream product

1101200-64-9Downstream Products

1101200-67-2 (7Z,10Z,13Z,16Z,19Z)-1-(2,4,6-trimethoxyphenyl)docosa-7,10,13,16,19-pentaen-2-yn-1-one

1101200-64-9Relevant academic research and scientific papers

First total synthesis of a polyunsaturated chromone metabolite isolated from the brown algae Zonaria tournefortii

Anwar, Many F.,Hansen, Trond Vidar

, p. 587 - 588 (2009)

(Chemical Equation Presented) Starting from the ethyl ester of eicosapentaenoic acid, the first total synthesis of the marine natural product all-(Z)-5,7-dihydroxy-2-(4Z,7Z,10Z,13Z,16Z-nonadecapentaenyl)chromone has been achieved in six steps and in 14% o

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