Cas 195515-46-9,N,N'-Bis[(1R)-2-chloro-1-phenylethyl]-2,2-diethyl-1,3-propanediamide

195515-46-9

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Basic information

Product Name: N,N'-Bis[(1R)-2-chloro-1-phenylethyl]-2,2-diethyl-1,3-propanediamide
Synonyms: N,N'-Bis[(1R)-2-chloro-1-phenylethyl]-2,2-diethyl-1,3-propanediamide
CAS NO:195515-46-9
Molecular Formula:
Molecular Weight: 435.394
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,N'-Bis[(1R)-2-chloro-1-phenylethyl]-2,2-diethyl-1,3-propanediamide(CAS DataBase Reference)
NIST Chemistry Reference: N,N'-Bis[(1R)-2-chloro-1-phenylethyl]-2,2-diethyl-1,3-propanediamide(195515-46-9)
EPA Substance Registry System: N,N'-Bis[(1R)-2-chloro-1-phenylethyl]-2,2-diethyl-1,3-propanediamide(195515-46-9)

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: 195515-46-9(Hazardous Substances Data)

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195515-46-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 195515-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,5,1 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 195515-46:
(8*1)+(7*9)+(6*5)+(5*5)+(4*1)+(3*5)+(2*4)+(1*6)=159
159 % 10 = 9
So 195515-46-9 is a valid CAS Registry Number.

195515-46-9Upstream product

195515-46-9Downstream Products

190791-28-7 (R)-4-phenyl-2-(3-((R)-4-phenyl-4,5-dihydrooxazol-2-yl)pentane-3-yl)-4,5-dihydrooxazole

195515-46-9Relevant academic research and scientific papers

Reactivity of 2-methylene-1,3-dicarbonyl compounds: Catalytic enantioselective Diels-Alder reaction

Yamauchi, Masashige,Aoki, Takashi,Li, Ming-Zhu,Honda, Yuko

, p. 3113 - 3118 (2001)

The catalytic enantioselective Diels-Alder reaction of 1,1-dicarbonylethenes 3 with cyclopentadiene in the presence of Ti-TADDOLs, Mg-Ph-box and Mg-Ph-mox complexes was investigated. Although both exo- and enantioselectivity with Ti-TADDOL catalysts were

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