Cas 123966-36-9,3.7.12.16-tetramethyl-1t.18t-bis-(5-hydroxyimino-2.2.6-trimethyl-cyclohexen-(6)-yl)-octadecanonaene-(1.3t.5t.7t.9t.11t.13t.15t.17)

123966-36-9

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Basic information

Product Name: 3.7.12.16-tetramethyl-1t.18t-bis-(5-hydroxyimino-2.2.6-trimethyl-cyclohexen-⁽⁶⁾-yl)-octadecanonaene-(1.3t.5t.7t.9t.11t.13t.15t.17)
Synonyms:
CAS NO:123966-36-9
Molecular Formula:
Molecular Weight: 594.881
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: 3.7.12.16-tetramethyl-1t.18t-bis-(5-hydroxyimino-2.2.6-trimethyl-cyclohexen-⁽⁶⁾-yl)-octadecanonaene-(1.3t.5t.7t.9t.11t.13t.15t.17)(CAS DataBase Reference)
NIST Chemistry Reference: 3.7.12.16-tetramethyl-1t.18t-bis-(5-hydroxyimino-2.2.6-trimethyl-cyclohexen-⁽⁶⁾-yl)-octadecanonaene-(1.3t.5t.7t.9t.11t.13t.15t.17)(123966-36-9)
EPA Substance Registry System: 3.7.12.16-tetramethyl-1t.18t-bis-(5-hydroxyimino-2.2.6-trimethyl-cyclohexen-⁽⁶⁾-yl)-octadecanonaene-(1.3t.5t.7t.9t.11t.13t.15t.17)(123966-36-9)

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: 123966-36-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 123966-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,9,6 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 123966-36:
(8*1)+(7*2)+(6*3)+(5*9)+(4*6)+(3*6)+(2*3)+(1*6)=139
139 % 10 = 9
So 123966-36-9 is a valid CAS Registry Number.

123966-36-9Upstream product

514-78-3 canthaxanthin

123966-36-9Downstream Products

123966-36-9Relevant academic research and scientific papers

Hydrophilic carotenoids: facile syntheses of carotenoid oxime hydrochlorides as long-chain, highly unsaturated cationic (bola)amphiphiles

Willibald, Julian,Rennebaum, Sandra,Breukers, Stefanie,Abdel Hafez, Shams H.,Patel, Anjan,pstad, Christer L.,Schmid, Rudolf,Naess, Stine Nalum,Sliwka, Hans-Richard,Partali, Vassilia

, p. 32 - 37 (2009)

Stable cationic carotenoid aggregates - predominantly of the J-type - develop when the hydrochlorides of carotenoid aldoximes and ketoximes are exposed to water. The oxime hydrochlorides are obtained by simple syntheses from commercially available food co

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