Cas 862890-47-9,ethyl 3-(4-fluorophenyl)-2-(4-methylphenylsulfonyloxy)-3-tert-butoxycarboxamidopropanoate

862890-47-9

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Basic information

Product Name: ethyl 3-(4-fluorophenyl)-2-(4-methylphenylsulfonyloxy)-3-tert-butoxycarboxamidopropanoate
Synonyms: ethyl 3-(4-fluorophenyl)-2-(4-methylphenylsulfonyloxy)-3-tert-butoxycarboxamidopropanoate
CAS NO:862890-47-9
Molecular Formula:
Molecular Weight: 481.542
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: ethyl 3-(4-fluorophenyl)-2-(4-methylphenylsulfonyloxy)-3-tert-butoxycarboxamidopropanoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 3-(4-fluorophenyl)-2-(4-methylphenylsulfonyloxy)-3-tert-butoxycarboxamidopropanoate(862890-47-9)
EPA Substance Registry System: ethyl 3-(4-fluorophenyl)-2-(4-methylphenylsulfonyloxy)-3-tert-butoxycarboxamidopropanoate(862890-47-9)

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: 862890-47-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 862890-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,8,9 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 862890-47:
(8*8)+(7*6)+(6*2)+(5*8)+(4*9)+(3*0)+(2*4)+(1*7)=209
209 % 10 = 9
So 862890-47-9 is a valid CAS Registry Number.

862890-47-9Upstream product

862890-47-9Downstream Products

862890-47-9Relevant academic research and scientific papers

Studies on stereoselective synthesis of ethyl anti-4-substituted phenyl-2-oxo-1,3-oxazolidine-5-carboxylates and their anti-bacterial activity

Madhusudhan,Om Reddy,Ramanatham,Dubey

, p. 2683 - 2688 (2007/10/03)

Ethyl anti-4-substituted phenyl-2-oxo-1,3-oxazolidine-5-carboxylates have been synthesized stereoselectively from N-Boc-β-amino alcohols by O-tosylation followed by SN2 cyclization. All the compounds prepared are tested for their in vitro anti-

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