Cas 1255461-41-6,dimethyl (2R,3R,4R)-3-(hydroxyamino)-4-(hydroxymethyl)-2-(4-methoxyphenyl)cyclopentane-1,1-dicarboxylate

1255461-41-6

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Basic information

Product Name: dimethyl (2R,3R,4R)-3-(hydroxyamino)-4-(hydroxymethyl)-2-(4-methoxyphenyl)cyclopentane-1,1-dicarboxylate
Synonyms: dimethyl (2R,3R,4R)-3-(hydroxyamino)-4-(hydroxymethyl)-2-(4-methoxyphenyl)cyclopentane-1,1-dicarboxylate
CAS NO:1255461-41-6
Molecular Formula:
Molecular Weight: 353.372
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: dimethyl (2R,3R,4R)-3-(hydroxyamino)-4-(hydroxymethyl)-2-(4-methoxyphenyl)cyclopentane-1,1-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl (2R,3R,4R)-3-(hydroxyamino)-4-(hydroxymethyl)-2-(4-methoxyphenyl)cyclopentane-1,1-dicarboxylate(1255461-41-6)
EPA Substance Registry System: dimethyl (2R,3R,4R)-3-(hydroxyamino)-4-(hydroxymethyl)-2-(4-methoxyphenyl)cyclopentane-1,1-dicarboxylate(1255461-41-6)

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: 1255461-41-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1255461-41-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,5,4,6 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1255461-41:
(9*1)+(8*2)+(7*5)+(6*5)+(5*4)+(4*6)+(3*1)+(2*4)+(1*1)=146
146 % 10 = 6
So 1255461-41-6 is a valid CAS Registry Number.

1255461-41-6Upstream product

1255460-82-2 dimethyl (2R,3E,4R)-3-(hydroxyimino)-4-(hydroxymethyl)-2-(4-methoxyphenyl)cyclopentane-1,1-dicarboxylate

1255461-41-6Downstream Products

1255461-41-6Relevant academic research and scientific papers

One-pot asymmetric cyclocarbohydroxylation sequence for the enantioselective synthesis of functionalised cyclopentanes

Raimondi, Wilfried,Lettieri, Gregory,Dulcere, Jean-Pierre,Bonne, Damien,Rodriguez, Jean

, p. 7247 - 7249 (2010)

A new method has been developed for the enantioselective synthesis of highly functionalised cyclopentanes bearing up to three stereogenic centres with very high stereoselectivity. This one-pot process combines an enantioselective organocatalytic Michael addition with a highly diastereoselective [3+2]-cycloaddition-fragmentation step.

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