Cas 1380096-59-2,(+)-(3R,1E,S(S))-1-phenyl-2-(p-tolylsulfinyl)pent-1-en-3-yl 2,2,2-trichloroacetimidate

1380096-59-2

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Basic information

Product Name: (+)-(3R,1E,S(S))-1-phenyl-2-(p-tolylsulfinyl)pent-1-en-3-yl 2,2,2-trichloroacetimidate
Synonyms: (+)-(3R,1E,S(S))-1-phenyl-2-(p-tolylsulfinyl)pent-1-en-3-yl 2,2,2-trichloroacetimidate
CAS NO:1380096-59-2
Molecular Formula:
Molecular Weight: 444.809
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: (+)-(3R,1E,S(S))-1-phenyl-2-(p-tolylsulfinyl)pent-1-en-3-yl 2,2,2-trichloroacetimidate(CAS DataBase Reference)
NIST Chemistry Reference: (+)-(3R,1E,S(S))-1-phenyl-2-(p-tolylsulfinyl)pent-1-en-3-yl 2,2,2-trichloroacetimidate(1380096-59-2)
EPA Substance Registry System: (+)-(3R,1E,S(S))-1-phenyl-2-(p-tolylsulfinyl)pent-1-en-3-yl 2,2,2-trichloroacetimidate(1380096-59-2)

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: 1380096-59-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1380096-59-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,0,9 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1380096-59:
(9*1)+(8*3)+(7*8)+(6*0)+(5*0)+(4*9)+(3*6)+(2*5)+(1*9)=162
162 % 10 = 2
So 1380096-59-2 is a valid CAS Registry Number.

1380096-59-2Upstream product

1380096-59-2Downstream Products

1380096-85-4 (+)-2,2,2-trichloro-N-((1R,2Z,S(S))-1-phenyl-2-(p-tolylsulfinyl)pent-2-en-1-yl)acetamide

1380096-59-2Relevant academic research and scientific papers

Sulfinyl-mediated stereoselective overman rearrangements and Diels-Alder cycloadditions

Fernández De La Pradilla, Roberto,Colomer, Ignacio,Viso, Alma

supporting information; experimental part, p. 3068 - 3071 (2012/08/07)

The Overman rearrangement of allylic sulfinyl trichloroacetimidates affords sulfinyl trichloroacetamides with high stereoselectivity and excellent yields. Bis-allylic substrates lead to amido 2-sulfinyl butadiene derivatives in excellent yields, with tota

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