Cas 1194510-06-9,N-[(R)-3-(3,4-dimethoxyphenyl)-2-methylpropylidene]-[(S)-2-methoxymethylpyrrolidin-1-yl]amine

1194510-06-9

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Basic information

Product Name: N-[(R)-3-(3,4-dimethoxyphenyl)-2-methylpropylidene]-[(S)-2-methoxymethylpyrrolidin-1-yl]amine
Synonyms: N-[(R)-3-(3,4-dimethoxyphenyl)-2-methylpropylidene]-[(S)-2-methoxymethylpyrrolidin-1-yl]amine
CAS NO:1194510-06-9
Molecular Formula:
Molecular Weight: 320.432
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: N-[(R)-3-(3,4-dimethoxyphenyl)-2-methylpropylidene]-[(S)-2-methoxymethylpyrrolidin-1-yl]amine(CAS DataBase Reference)
NIST Chemistry Reference: N-[(R)-3-(3,4-dimethoxyphenyl)-2-methylpropylidene]-[(S)-2-methoxymethylpyrrolidin-1-yl]amine(1194510-06-9)
EPA Substance Registry System: N-[(R)-3-(3,4-dimethoxyphenyl)-2-methylpropylidene]-[(S)-2-methoxymethylpyrrolidin-1-yl]amine(1194510-06-9)

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: 1194510-06-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1194510-06-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,4,5,1 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1194510-06:
(9*1)+(8*1)+(7*9)+(6*4)+(5*5)+(4*1)+(3*0)+(2*0)+(1*6)=139
139 % 10 = 9
So 1194510-06-9 is a valid CAS Registry Number.

1194510-06-9Upstream product

1194509-73-3 N-[3-(3,4-dimethoxyphenyl)propylidene]-[(S)-2-methoxymethylpyrrolidin-1-yl]amine

1194510-06-9Downstream Products

1194510-06-9Relevant academic research and scientific papers

Asymmetric synthesis of 3- or 4-alkyl or arylbenzo[c]azepines

Dumoulin, David,Lebrun, Stephane,Couture, Axel,Deniau, Eric,Grandclaudon, Pierre

, p. 1903 - 1911 (2009)

Two flexible routes for the stereoselective synthesis of a variety of 3- or 4-alkylated or arylated tetrahydrobenzazepines have been developed. The key steps are the highly diastereoselective metallation/alkylation reaction and 1,2-addition processes applied to stereopure SAMP hydrazones combined with a cyclomethylenation reaction.

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