Cas 1055309-75-5,(4R,5R)-2-((1S,6R)-6-sec-butyl-1-methylcyclohexa-2,4-dienyl)-4,5-diphenyloxazoline

1055309-75-5

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Basic information

Product Name: (4R,5R)-2-((1S,6R)-6-sec-butyl-1-methylcyclohexa-2,4-dienyl)-4,5-diphenyloxazoline
Synonyms: (4R,5R)-2-((1S,6R)-6-sec-butyl-1-methylcyclohexa-2,4-dienyl)-4,5-diphenyloxazoline
CAS NO:1055309-75-5
Molecular Formula:
Molecular Weight: 371.522
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: (4R,5R)-2-((1S,6R)-6-sec-butyl-1-methylcyclohexa-2,4-dienyl)-4,5-diphenyloxazoline(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5R)-2-((1S,6R)-6-sec-butyl-1-methylcyclohexa-2,4-dienyl)-4,5-diphenyloxazoline(1055309-75-5)
EPA Substance Registry System: (4R,5R)-2-((1S,6R)-6-sec-butyl-1-methylcyclohexa-2,4-dienyl)-4,5-diphenyloxazoline(1055309-75-5)

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: 1055309-75-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1055309-75-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,5,3,0 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1055309-75:
(9*1)+(8*0)+(7*5)+(6*5)+(5*3)+(4*0)+(3*9)+(2*7)+(1*5)=135
135 % 10 = 5
So 1055309-75-5 is a valid CAS Registry Number.

1055309-75-5Upstream product

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1055309-75-5Relevant academic research and scientific papers

Stereoselective dearomatizing addition of nucleophiles to uncomplexed benzene rings: A route to carbocyclic sugar analogues

Clayden, Jonathan,Parris, Sean,Cabedo, Nuria,Payne, Andrew H.

supporting information; experimental part, p. 5060 - 5062 (2009/03/11)

(Chemical Equation Presented) Versatile synthetic intermediates were formed by the dearomatization of 2-aryl 4,5-diphenyloxazolines with secondary alkyl lithium reagents in the presence of N,N′-dimethylpropyleneurea (DMPU; see scheme). The resulting cyclo

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