Cas 1343483-10-2,(2S)-2-{(E)-[(2-hydroxynaphthalen-1-yl)methylidene]amino}-1,1,4,4-tetraphenylbutane-1,4-diol

1343483-10-2

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Basic information

Product Name: (2S)-2-{(E)-[(2-hydroxynaphthalen-1-yl)methylidene]amino}-1,1,4,4-tetraphenylbutane-1,4-diol
Synonyms:
CAS NO:1343483-10-2
Molecular Formula:
Molecular Weight: 563.696
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-{(E)-[(2-hydroxynaphthalen-1-yl)methylidene]amino}-1,1,4,4-tetraphenylbutane-1,4-diol(CAS DataBase Reference)
NIST Chemistry Reference: (2S)-2-{(E)-[(2-hydroxynaphthalen-1-yl)methylidene]amino}-1,1,4,4-tetraphenylbutane-1,4-diol(1343483-10-2)
EPA Substance Registry System: (2S)-2-{(E)-[(2-hydroxynaphthalen-1-yl)methylidene]amino}-1,1,4,4-tetraphenylbutane-1,4-diol(1343483-10-2)

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: 1343483-10-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1343483-10-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,3,4,8 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1343483-10:
(9*1)+(8*3)+(7*4)+(6*3)+(5*4)+(4*8)+(3*3)+(2*1)+(1*0)=142
142 % 10 = 2
So 1343483-10-2 is a valid CAS Registry Number.

1343483-10-2Upstream product

708-06-5 2-hydroxynaphthalene-1-carbaldehyde

1343483-10-2Downstream Products

1343483-10-2Relevant academic research and scientific papers

Enantioselective Henry reaction catalyzed by a novel L-(+)-aspartic acid-derived Schiff base ligand and Cu(II) ion

Koz, Gamze,Astley, Demet,Astley, Stephen Thomas

, p. 553 - 560 (2011)

Mild and efficient enantioselective Henry reactions of nitromethane with various aldehydes were catalyzed by a novel L-(+)-aspartic acid-derived Schiff base ligand in the presence of Cu(II) ions, affording the corresponding adducts in high yields (up to 96%) and enantioselectivities (up to 92% ee). TUBITAK.

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