Cas 1403680-41-0,(4R,4aR,8aS)-methyl 4-(4-chlorophenyl)-8a-hydroxy-4a-nitro-4a,5,6,7,8,8a-hexahydro-4H-chromene-2-carboxylate

1403680-41-0

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Product Name: (4R,4aR,8aS)-methyl 4-(4-chlorophenyl)-8a-hydroxy-4a-nitro-4a,5,6,7,8,8a-hexahydro-4H-chromene-2-carboxylate
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CAS NO:1403680-41-0
Molecular Formula:
Molecular Weight: 367.786
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
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Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
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Solubility: N/A
CAS DataBase Reference: (4R,4aR,8aS)-methyl 4-(4-chlorophenyl)-8a-hydroxy-4a-nitro-4a,5,6,7,8,8a-hexahydro-4H-chromene-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (4R,4aR,8aS)-methyl 4-(4-chlorophenyl)-8a-hydroxy-4a-nitro-4a,5,6,7,8,8a-hexahydro-4H-chromene-2-carboxylate(1403680-41-0)
EPA Substance Registry System: (4R,4aR,8aS)-methyl 4-(4-chlorophenyl)-8a-hydroxy-4a-nitro-4a,5,6,7,8,8a-hexahydro-4H-chromene-2-carboxylate(1403680-41-0)

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RTECS:
HazardClass: N/A
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Hazardous Substances Data: 1403680-41-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1403680-41-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,6,8 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1403680-41:
(9*1)+(8*4)+(7*0)+(6*3)+(5*6)+(4*8)+(3*0)+(2*4)+(1*1)=130
130 % 10 = 0
So 1403680-41-0 is a valid CAS Registry Number.

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1403680-41-0Relevant academic research and scientific papers

Asymmetric inverse-electron-demand hetero-diels-alder reaction for the construction of bicyclic skeletons with multiple stereocenters by using a bifunctional organocatalytic strategy: An efficient approach to chiral macrolides

Jiang, Xianxing,Wang, Long,Kai, Ming,Zhu, Liping,Yao, Xiaojun,Wang, Rui

supporting information, p. 11465 - 11473,9 (2012/12/11)

We have performed the first bifunctional organocatalytic highly enantioselective inverse-electron-demand hetero-Diels-Alder reaction of cyclic ketones with enones to afford densely functionalized bicyclic skeletons that contain three stereocenters (up 82 % yield, 10:1 d.r., and 97 % ee). Unlike the previous IEDDAR catalytic strategy, this method features a double HOMO dienophile/ LUMOdiene-activated pathway. Moreover, this process provides a promising method for the construction of enantioenriched macrolides. Bicyclic exercises: A highly enantioselective inverse-electron- demand hetero-Diels-Alder reaction of cyclic ketones with enones affords functionalized bicyclic skeletons with three stereocenters that can be used for the construction of macrolides. Copyright

Asymmetric inverse-electron-demand hetero-diels-alder reaction for the construction of bicyclic skeletons with multiple stereocenters by using a bifunctional organocatalytic strategy: An efficient approach to chiral macrolides

Jiang, Xianxing,Wang, Long,Kai, Ming,Zhu, Liping,Yao, Xiaojun,Wang, Rui

supporting information, p. 11465 - 11473 (2013/01/14)

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