Cas 346408-90-0,(3S,4R)-methyl 3-acetyl-4-[3-(cyclopentyloxy)-4-methoxyphenyl]-3-methylpyrrolidine-1-carboxylate

346408-90-0

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Basic information

Product Name: (3S,4R)-methyl 3-acetyl-4-[3-(cyclopentyloxy)-4-methoxyphenyl]-3-methylpyrrolidine-1-carboxylate
Synonyms:
CAS NO:346408-90-0
Molecular Formula:
Molecular Weight: 375.465
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: (3S,4R)-methyl 3-acetyl-4-[3-(cyclopentyloxy)-4-methoxyphenyl]-3-methylpyrrolidine-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4R)-methyl 3-acetyl-4-[3-(cyclopentyloxy)-4-methoxyphenyl]-3-methylpyrrolidine-1-carboxylate(346408-90-0)
EPA Substance Registry System: (3S,4R)-methyl 3-acetyl-4-[3-(cyclopentyloxy)-4-methoxyphenyl]-3-methylpyrrolidine-1-carboxylate(346408-90-0)

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: 346408-90-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 346408-90-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,6,4,0 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 346408-90:
(8*3)+(7*4)+(6*6)+(5*4)+(4*0)+(3*8)+(2*9)+(1*0)=150
150 % 10 = 0
So 346408-90-0 is a valid CAS Registry Number.

346408-90-0Upstream product

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346408-90-0Relevant academic research and scientific papers

Stereocontrolled construction of quaternary stereocenters by inter- and intramolecular nitro-michael additions catalyzed by bifunctional thioureas

Manzano, Ruben,Andres, Jose M.,Muruzabal, Maria D.,Pedrosa, Rafael

experimental part, p. 3364 - 3372 (2011/03/17)

A highly diastereo- and enantioselective conjugate addition of β-keto esters to nitroolefins, catalyzed by a chiral thiourea prepared from L-valine is described. The formation of two contiguous tertiary and quaternary stereocenters occurs in high yield an

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