Cas 1401467-75-1,1-((S)-3,3-dimethyl-1-oxo-1-((R)-2-(phenanthren-9-yl)pyrrolidin-1-yl)butan-2-yl)-3-((1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexyl)thiourea

1401467-75-1

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Basic information

Product Name: 1-((S)-3,3-dimethyl-1-oxo-1-((R)-2-(phenanthren-9-yl)pyrrolidin-1-yl)butan-2-yl)-3-((1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexyl)thiourea
Synonyms:
CAS NO:1401467-75-1
Molecular Formula:
Molecular Weight: 656.935
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-((S)-3,3-dimethyl-1-oxo-1-((R)-2-(phenanthren-9-yl)pyrrolidin-1-yl)butan-2-yl)-3-((1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexyl)thiourea(CAS DataBase Reference)
NIST Chemistry Reference: 1-((S)-3,3-dimethyl-1-oxo-1-((R)-2-(phenanthren-9-yl)pyrrolidin-1-yl)butan-2-yl)-3-((1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexyl)thiourea(1401467-75-1)
EPA Substance Registry System: 1-((S)-3,3-dimethyl-1-oxo-1-((R)-2-(phenanthren-9-yl)pyrrolidin-1-yl)butan-2-yl)-3-((1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexyl)thiourea(1401467-75-1)

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Safety Statements: N/A
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RTECS:
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Hazardous Substances Data: 1401467-75-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1401467-75-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,4,6 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1401467-75:
(9*1)+(8*4)+(7*0)+(6*1)+(5*4)+(4*6)+(3*7)+(2*7)+(1*5)=131
131 % 10 = 1
So 1401467-75-1 is a valid CAS Registry Number.

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1401467-75-1Relevant academic research and scientific papers

Enantioselective thiourea-catalyzed intramolecular cope-type hydroamination

Brown, Adam R.,Uyeda, Christopher,Brotherton, Carolyn A.,Jacobsen, Eric N.

, p. 6747 - 6749 (2013/06/05)

Catalysis of Cope-type rearrangements of bis-homoallylic hydroxylamines is demonstrated using chiral thiourea derivatives. This formal intramolecular hydroamination reaction provides access to highly enantioenriched α-substituted pyrrolidine products and represents a complementary approach to metal-catalyzed methods.

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