Cas 214139-72-7,(3R,3aR,6R,6aR)-3,6-Bis-(2-fluoro-benzyloxy)-tetrahydro-furo[3,2-b]furan-2,5-dione

214139-72-7

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Basic information

Product Name: (3R,3aR,6R,6aR)-3,6-Bis-(2-fluoro-benzyloxy)-tetrahydro-furo[3,2-b]furan-2,5-dione
Synonyms: (3R,3aR,6R,6aR)-3,6-Bis-(2-fluoro-benzyloxy)-tetrahydro-furo[3,2-b]furan-2,5-dione
CAS NO:214139-72-7
Molecular Formula:
Molecular Weight: 390.34
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,3aR,6R,6aR)-3,6-Bis-(2-fluoro-benzyloxy)-tetrahydro-furo[3,2-b]furan-2,5-dione(CAS DataBase Reference)
NIST Chemistry Reference: (3R,3aR,6R,6aR)-3,6-Bis-(2-fluoro-benzyloxy)-tetrahydro-furo[3,2-b]furan-2,5-dione(214139-72-7)
EPA Substance Registry System: (3R,3aR,6R,6aR)-3,6-Bis-(2-fluoro-benzyloxy)-tetrahydro-furo[3,2-b]furan-2,5-dione(214139-72-7)

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: 214139-72-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 214139-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,1,3 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 214139-72:
(8*2)+(7*1)+(6*4)+(5*1)+(4*3)+(3*9)+(2*7)+(1*2)=107
107 % 10 = 7
So 214139-72-7 is a valid CAS Registry Number.

214139-72-7Upstream product

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214139-72-7Relevant academic research and scientific papers

Design and synthesis of potent C2-symmetric diol-based HIV-1 protease inhibitors: Effects of fluoro substitution

Pyring,Lindberg,Rosenquist,Zuccarello,Kvarnstr?m,Zhang,Vrang,Unge,Classon,Hallberg,Samuelsson

, p. 3083 - 3091 (2007/10/03)

Implementation of derivatized carbohydrates as C2-symmetric HIV-1 protease inhibitors has previously been reported. With the objective of improving the anti-HIV activity of such compounds, we synthesized a series of fluoro substituted P1/P1′ an

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