Cas 1404096-03-2,(2S,2'S)-N,N'-[(2S,3S)-1,4-bis(benzyloxy)butane-2,3-diyl]bis[2-(6-methoxy-2-naphthyl)propanamide]

1404096-03-2

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Basic information

Product Name: (2S,2'S)-N,N'-[(2S,3S)-1,4-bis(benzyloxy)butane-2,3-diyl]bis[2-(6-methoxy-2-naphthyl)propanamide]
Synonyms: (2S,2'S)-N,N'-[(2S,3S)-1,4-bis(benzyloxy)butane-2,3-diyl]bis[2-(6-methoxy-2-naphthyl)propanamide]
CAS NO:1404096-03-2
Molecular Formula:
Molecular Weight: 724.897
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'S)-N,N'-[(2S,3S)-1,4-bis(benzyloxy)butane-2,3-diyl]bis[2-(6-methoxy-2-naphthyl)propanamide](CAS DataBase Reference)
NIST Chemistry Reference: (2S,2'S)-N,N'-[(2S,3S)-1,4-bis(benzyloxy)butane-2,3-diyl]bis[2-(6-methoxy-2-naphthyl)propanamide](1404096-03-2)
EPA Substance Registry System: (2S,2'S)-N,N'-[(2S,3S)-1,4-bis(benzyloxy)butane-2,3-diyl]bis[2-(6-methoxy-2-naphthyl)propanamide](1404096-03-2)

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: 1404096-03-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1404096-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,4,0,9 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1404096-03:
(9*1)+(8*4)+(7*0)+(6*4)+(5*0)+(4*9)+(3*6)+(2*0)+(1*3)=122
122 % 10 = 2
So 1404096-03-2 is a valid CAS Registry Number.

1404096-03-2Upstream product

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1404096-03-2Relevant academic research and scientific papers

Asymmetric henry reaction catalyzed by novel chiral bioxazolines from tartaric acid

Balaraman, Kaluvu,Vasanthan, Ravichandran,Kesavan, Venkitasamy

experimental part, p. 2455 - 2462 (2012/09/21)

Novel C2-symmetric chiral bioxazolines were synthesized in good yields by the fusion of optically active acids with a tartaric acid derivative. Complexes of these products with copper(II) acetate monohydrate were found to be excellent catalysts

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