Cas 506441-83-4,(2S,2'R)-N-[2'-(methoxymethyl)pyrrolidin-1'-yl]-N-(1,1,1-trifluoropent-4-en-2-yl)benzamide

506441-83-4

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Basic information

Product Name: (2S,2'R)-N-[2'-(methoxymethyl)pyrrolidin-1'-yl]-N-(1,1,1-trifluoropent-4-en-2-yl)benzamide
Synonyms: (2S,2'R)-N-[2'-(methoxymethyl)pyrrolidin-1'-yl]-N-(1,1,1-trifluoropent-4-en-2-yl)benzamide
CAS NO:506441-83-4
Molecular Formula:
Molecular Weight: 356.388
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: (2S,2'R)-N-[2'-(methoxymethyl)pyrrolidin-1'-yl]-N-(1,1,1-trifluoropent-4-en-2-yl)benzamide(CAS DataBase Reference)
NIST Chemistry Reference: (2S,2'R)-N-[2'-(methoxymethyl)pyrrolidin-1'-yl]-N-(1,1,1-trifluoropent-4-en-2-yl)benzamide(506441-83-4)
EPA Substance Registry System: (2S,2'R)-N-[2'-(methoxymethyl)pyrrolidin-1'-yl]-N-(1,1,1-trifluoropent-4-en-2-yl)benzamide(506441-83-4)

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: 506441-83-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 506441-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,6,4,4 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 506441-83:
(8*5)+(7*0)+(6*6)+(5*4)+(4*4)+(3*1)+(2*8)+(1*3)=134
134 % 10 = 4
So 506441-83-4 is a valid CAS Registry Number.

506441-83-4Upstream product

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506441-83-4Relevant academic research and scientific papers

Asymmetric synthesis of both enantiomers of α-trifluoromethyl substituted homoallylamine

Funabiki, Kazumasa,Nagamori, Masashi,Matsui, Masaki,Enders, Dieter

, p. 2585 - 2588 (2002)

An efficient asymmetric synthesis of both enantiomers of α-trifluoromethylated homoallylamine via nucleophilic allylation of trifluoroacetaldehyde SAMP- or RAMP-hydrazone, followed by benzoylation and SmI2-promoted nitrogen-nitrogen single bond cleavage is described.

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