Cas 1322075-92-2,4-hydroxy-3-((S,2E,4E,6E)-8-(hydroxymethyl)deca-2,4,6-trienoyl)-5-(4-hydroxyphenyl) pyridin-2(1H)-one

1322075-92-2

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Basic information

Product Name: 4-hydroxy-3-((S,2E,4E,6E)-8-(hydroxymethyl)deca-2,4,6-trienoyl)-5-(4-hydroxyphenyl) pyridin-2(1H)-one
Synonyms: 4-hydroxy-3-((S,2E,4E,6E)-8-(hydroxymethyl)deca-2,4,6-trienoyl)-5-(4-hydroxyphenyl) pyridin-2(1H)-one
CAS NO:1322075-92-2
Molecular Formula:
Molecular Weight: 381.428
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: 4-hydroxy-3-((S,2E,4E,6E)-8-(hydroxymethyl)deca-2,4,6-trienoyl)-5-(4-hydroxyphenyl) pyridin-2(1H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 4-hydroxy-3-((S,2E,4E,6E)-8-(hydroxymethyl)deca-2,4,6-trienoyl)-5-(4-hydroxyphenyl) pyridin-2(1H)-one(1322075-92-2)
EPA Substance Registry System: 4-hydroxy-3-((S,2E,4E,6E)-8-(hydroxymethyl)deca-2,4,6-trienoyl)-5-(4-hydroxyphenyl) pyridin-2(1H)-one(1322075-92-2)

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: 1322075-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1322075-92-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,2,0,7 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1322075-92:
(9*1)+(8*3)+(7*2)+(6*2)+(5*0)+(4*7)+(3*5)+(2*9)+(1*2)=122
122 % 10 = 2
So 1322075-92-2 is a valid CAS Registry Number.

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1322075-92-2Relevant academic research and scientific papers

Catalytic enantioselective total synthesis of (+)-torrubiellone C

Jessen, Henning J.,Schumacher, Andreas,Schmid, Fabian,Pfaltz, Andreas,Gademann, Karl

, p. 4368 - 4370 (2011)

Silyl-protected (R)-methyl 2-(hydroxymethyl)butanoate was obtained by an enantioselective Ir-catalyzed hydrogenation in high yield and selectivity. Elaboration of this building block via Takai and Stille reactions gave a protected hydroxy polyene chain, w

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