Cas 959979-72-7,(S)-N-benzhydryl-N,3,3-trimethyl-2-(3-((1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexyl)thioureido)butanamide

959979-72-7

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Basic information

Product Name: (S)-N-benzhydryl-N,3,3-trimethyl-2-(3-((1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexyl)thioureido)butanamide
Synonyms:
CAS NO:959979-72-7
Molecular Formula:
Molecular Weight: 606.875
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: (S)-N-benzhydryl-N,3,3-trimethyl-2-(3-((1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexyl)thioureido)butanamide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N-benzhydryl-N,3,3-trimethyl-2-(3-((1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexyl)thioureido)butanamide(959979-72-7)
EPA Substance Registry System: (S)-N-benzhydryl-N,3,3-trimethyl-2-(3-((1R,2R)-2-(2-methyl-5-phenyl-1H-pyrrol-1-yl)cyclohexyl)thioureido)butanamide(959979-72-7)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 959979-72-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 959979-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,9,7 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 959979-72:
(8*9)+(7*5)+(6*9)+(5*9)+(4*7)+(3*9)+(2*7)+(1*2)=277
277 % 10 = 7
So 959979-72-7 is a valid CAS Registry Number.

959979-72-7Upstream product

959979-72-7Downstream Products

959979-72-7Relevant 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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