Cas 1222922-63-5,1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-3,3-dimethyl-1-oxo-1-((R)-2-(pyren-4-yl)pyrrolidin-1-yl)butan-2-yl)thiourea

1222922-63-5

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Basic information

Product Name: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-3,3-dimethyl-1-oxo-1-((R)-2-(pyren-4-yl)pyrrolidin-1-yl)butan-2-yl)thiourea
Synonyms:
CAS NO:1222922-63-5
Molecular Formula:
Molecular Weight: 655.707
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: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-3,3-dimethyl-1-oxo-1-((R)-2-(pyren-4-yl)pyrrolidin-1-yl)butan-2-yl)thiourea(CAS DataBase Reference)
NIST Chemistry Reference: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-3,3-dimethyl-1-oxo-1-((R)-2-(pyren-4-yl)pyrrolidin-1-yl)butan-2-yl)thiourea(1222922-63-5)
EPA Substance Registry System: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((S)-3,3-dimethyl-1-oxo-1-((R)-2-(pyren-4-yl)pyrrolidin-1-yl)butan-2-yl)thiourea(1222922-63-5)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1222922-63-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1222922-63-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,2,9,2 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1222922-63:
(9*1)+(8*2)+(7*2)+(6*2)+(5*9)+(4*2)+(3*2)+(2*6)+(1*3)=125
125 % 10 = 5
So 1222922-63-5 is a valid CAS Registry Number.

1222922-63-5Upstream product

23165-29-9 3,5-bistrifluoromethylphenylisothiocyanate

1222922-63-5Downstream Products

1222922-63-5Relevant academic research and scientific papers

Enantioselective thiourea-catalyzed cationic polycyclizations

Knowles, Robert R.,Lin, Song,Jacobsen, Eric N.

, p. 5030 - 5032 (2010)

A new thiourea catalyst is reported for the enantioselective cationic polycyclization of hydroxylactams. Both the yield and enantioselectivity of this transformation were found to vary strongly with the identity of a single aromatic residue on a common ca

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