Cas 1210360-52-3,1-(3,5-bis(trifluoromethyl)phenyl)-3-((1S,2R)-2-(triisopropylsilyloxy)-2,3-dihydro-1H-inden-1-yl)thiourea

1210360-52-3

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Basic information

Product Name: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((1S,2R)-2-(triisopropylsilyloxy)-2,3-dihydro-1H-inden-1-yl)thiourea
Synonyms: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((1S,2R)-2-(triisopropylsilyloxy)-2,3-dihydro-1H-inden-1-yl)thiourea
CAS NO:1210360-52-3
Molecular Formula:
Molecular Weight: 576.722
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-((1S,2R)-2-(triisopropylsilyloxy)-2,3-dihydro-1H-inden-1-yl)thiourea(CAS DataBase Reference)
NIST Chemistry Reference: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((1S,2R)-2-(triisopropylsilyloxy)-2,3-dihydro-1H-inden-1-yl)thiourea(1210360-52-3)
EPA Substance Registry System: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((1S,2R)-2-(triisopropylsilyloxy)-2,3-dihydro-1H-inden-1-yl)thiourea(1210360-52-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1210360-52-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1210360-52-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,0,3,6 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1210360-52:
(9*1)+(8*2)+(7*1)+(6*0)+(5*3)+(4*6)+(3*0)+(2*5)+(1*2)=83
83 % 10 = 3
So 1210360-52-3 is a valid CAS Registry Number.

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1210360-52-3Relevant academic research and scientific papers

Acyl Phosphonates: Good hydrogen bond acceptors and ester/amide equivalents in asymmetric organocatalysis

Jiang, Hao,Paixao, Marcio W.,Monge, David,Jorgensen, Karl Anker

supporting information; experimental part, p. 2775 - 2783 (2010/06/11)

This study demonstrates that unsaturated acyl phosphonates are excellent hydrogen-bond acceptors in enantioselective organocatalysis. By employing chiral thioureas orsquaramides as catalysts, the acyl phosphonates are effectively coordinated and activated

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