Cas 207598-56-9,(2R,4aR,5aR,8aR,8bS)-3-Isopropyl-7,7-dimethyl-2-(4-nitro-phenoxy)-hexahydro-[1,3]dioxolo[4,5]furo[2,3-e][1,3,2]oxazaphosphinine

207598-56-9

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Basic information

Product Name: (2R,4aR,5aR,8aR,8bS)-3-Isopropyl-7,7-dimethyl-2-(4-nitro-phenoxy)-hexahydro-[1,3]dioxolo[4,5]furo[2,3-e][1,3,2]oxazaphosphinine
Synonyms: (2R,4aR,5aR,8aR,8bS)-3-Isopropyl-7,7-dimethyl-2-(4-nitro-phenoxy)-hexahydro-[1,3]dioxolo[4,5]furo[2,3-e][1,3,2]oxazaphosphinine
CAS NO:207598-56-9
Molecular Formula:
Molecular Weight: 398.353
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: (2R,4aR,5aR,8aR,8bS)-3-Isopropyl-7,7-dimethyl-2-(4-nitro-phenoxy)-hexahydro-[1,3]dioxolo[4,5]furo[2,3-e][1,3,2]oxazaphosphinine(CAS DataBase Reference)
NIST Chemistry Reference: (2R,4aR,5aR,8aR,8bS)-3-Isopropyl-7,7-dimethyl-2-(4-nitro-phenoxy)-hexahydro-[1,3]dioxolo[4,5]furo[2,3-e][1,3,2]oxazaphosphinine(207598-56-9)
EPA Substance Registry System: (2R,4aR,5aR,8aR,8bS)-3-Isopropyl-7,7-dimethyl-2-(4-nitro-phenoxy)-hexahydro-[1,3]dioxolo[4,5]furo[2,3-e][1,3,2]oxazaphosphinine(207598-56-9)

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: 207598-56-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 207598-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,5,9 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 207598-56:
(8*2)+(7*0)+(6*7)+(5*5)+(4*9)+(3*8)+(2*5)+(1*6)=159
159 % 10 = 9
So 207598-56-9 is a valid CAS Registry Number.

207598-56-9Upstream product

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207598-56-9Relevant academic research and scientific papers

Stereoselective synthesis of dithymidine phosphorothioates using xylose derivatives as chiral auxiliaries

Jin, Yi,Just, George

, p. 3647 - 3654 (1998)

1,2-O-Cyclopentylidene-5-deoxy-5-isopropylamino-α-D-xylofuranose 1 and its enantiomer 11 were used as chiral auxiliaries to form, respectively, Sp and Rp dithymidine phosphorothioates 9 and 10 in 98% diastereomeric excess, using phosphoramidite methodology and 2-bromo-4,5-dicyanoimidazole as catalyst. The stereochemistry of the coupling reaction is discussed.

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