Cas 1136890-03-3,(2S,5S)-2-tert-butyl-5-((Z)-3,3,3-trifluoroprop-1-enyl)-5-phenyl-1,3-dioxolan-4-one

1136890-03-3

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Basic information

Product Name: (2S,5S)-2-tert-butyl-5-((Z)-3,3,3-trifluoroprop-1-enyl)-5-phenyl-1,3-dioxolan-4-one
Synonyms: (2S,5S)-2-tert-butyl-5-((Z)-3,3,3-trifluoroprop-1-enyl)-5-phenyl-1,3-dioxolan-4-one
CAS NO:1136890-03-3
Molecular Formula:
Molecular Weight: 314.304
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: (2S,5S)-2-tert-butyl-5-((Z)-3,3,3-trifluoroprop-1-enyl)-5-phenyl-1,3-dioxolan-4-one(CAS DataBase Reference)
NIST Chemistry Reference: (2S,5S)-2-tert-butyl-5-((Z)-3,3,3-trifluoroprop-1-enyl)-5-phenyl-1,3-dioxolan-4-one(1136890-03-3)
EPA Substance Registry System: (2S,5S)-2-tert-butyl-5-((Z)-3,3,3-trifluoroprop-1-enyl)-5-phenyl-1,3-dioxolan-4-one(1136890-03-3)

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: 1136890-03-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1136890-03-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,6,8,9 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1136890-03:
(9*1)+(8*1)+(7*3)+(6*6)+(5*8)+(4*9)+(3*0)+(2*0)+(1*3)=153
153 % 10 = 3
So 1136890-03-3 is a valid CAS Registry Number.

1136890-03-3Upstream product

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1136890-03-3Relevant academic research and scientific papers

Diastereoselective room-temperature Pd-catalyzed α-arylation and vinylation of arylmandelic acid derivatives

Jiang, Lei,Weist, Stefan,Jansat, Susanna

supporting information; experimental part, p. 1543 - 1546 (2009/09/06)

Palladium-catalyzed α-arylation and vinylation of dioxolane (S,S)-I, easily obtained from (S)-mandelic acid, proceeds with high yields and excellent diastereoselectivity at room temperature employing commercially available P(t-Bu)3·HBF4/s

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