Cas 503552-79-2,methyl (3S,6S,7R,7aR)-7-(4-fluorophenyl)-3-phenyl-5-oxo-tetrahydro-1H,3H-pyrrolo[1,2-c]oxazole-6-carboxylate

503552-79-2

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Basic information

Product Name: methyl (3S,6S,7R,7aR)-7-(4-fluorophenyl)-3-phenyl-5-oxo-tetrahydro-1H,3H-pyrrolo[1,2-c]oxazole-6-carboxylate
Synonyms: methyl (3S,6S,7R,7aR)-7-(4-fluorophenyl)-3-phenyl-5-oxo-tetrahydro-1H,3H-pyrrolo[1,2-c]oxazole-6-carboxylate
CAS NO:503552-79-2
Molecular Formula:
Molecular Weight: 355.366
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: methyl (3S,6S,7R,7aR)-7-(4-fluorophenyl)-3-phenyl-5-oxo-tetrahydro-1H,3H-pyrrolo[1,2-c]oxazole-6-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (3S,6S,7R,7aR)-7-(4-fluorophenyl)-3-phenyl-5-oxo-tetrahydro-1H,3H-pyrrolo[1,2-c]oxazole-6-carboxylate(503552-79-2)
EPA Substance Registry System: methyl (3S,6S,7R,7aR)-7-(4-fluorophenyl)-3-phenyl-5-oxo-tetrahydro-1H,3H-pyrrolo[1,2-c]oxazole-6-carboxylate(503552-79-2)

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: 503552-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 503552-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,5,5 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 503552-79:
(8*5)+(7*0)+(6*3)+(5*5)+(4*5)+(3*2)+(2*7)+(1*9)=132
132 % 10 = 2
So 503552-79-2 is a valid CAS Registry Number.

503552-79-2Upstream product

503552-79-2Downstream Products

503552-80-5 (2S,3R,4S)-1-benzyl-3-(4-fluorophenyl)pyrrolidine-2,4-bismethanol

503552-79-2Relevant academic research and scientific papers

A formal synthesis of (-)-paroxetine by enantioselective ring enlargement of a trisubstituted prolinol

Cossy, Janine,Mirguet, Olivier,Pardo, Domingo Gomez,Desmurs, Jean-Roger

, p. 3543 - 3551 (2007/10/03)

A ring expansion and a radical dehalogenation have been used as the key steps in a formal total synthesis of (-)-paroxetine. The substituted piperidine ring precursor of (-)-paroxetine was generated by means of a stereoselective ring expansion of prolinol. ( Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002).

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