Cas 258826-41-4,Dibenzyl-{(E)-(1S,2R)-1-isopropyl-2-[2-(2-methoxy-ethoxymethoxy)-ethyl]-4-methyl-hexa-3,5-dienyl}-amine

258826-41-4

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Basic information

Product Name: Dibenzyl-{(E)-(1S,2R)-1-isopropyl-2-[2-(2-methoxy-ethoxymethoxy)-ethyl]-4-methyl-hexa-3,5-dienyl}-amine
Synonyms: Dibenzyl-{(E)-(1S,2R)-1-isopropyl-2-[2-(2-methoxy-ethoxymethoxy)-ethyl]-4-methyl-hexa-3,5-dienyl}-amine
CAS NO:258826-41-4
Molecular Formula:
Molecular Weight: 465.676
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: Dibenzyl-{(E)-(1S,2R)-1-isopropyl-2-[2-(2-methoxy-ethoxymethoxy)-ethyl]-4-methyl-hexa-3,5-dienyl}-amine(CAS DataBase Reference)
NIST Chemistry Reference: Dibenzyl-{(E)-(1S,2R)-1-isopropyl-2-[2-(2-methoxy-ethoxymethoxy)-ethyl]-4-methyl-hexa-3,5-dienyl}-amine(258826-41-4)
EPA Substance Registry System: Dibenzyl-{(E)-(1S,2R)-1-isopropyl-2-[2-(2-methoxy-ethoxymethoxy)-ethyl]-4-methyl-hexa-3,5-dienyl}-amine(258826-41-4)

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: 258826-41-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 258826-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,8,8,2 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 258826-41:
(8*2)+(7*5)+(6*8)+(5*8)+(4*2)+(3*6)+(2*4)+(1*1)=174
174 % 10 = 4
So 258826-41-4 is a valid CAS Registry Number.

258826-41-4Upstream product

258826-41-4Downstream Products

258826-41-4Relevant academic research and scientific papers

Chemoselective oxidative debenzylation of N,N-dibenzylamines

Hungerhoff, Benno,Samanta, Subhendu S.,Roels, Jochen,Metz, Peter

, p. 77 - 79 (2007/10/03)

Tertiary amines incorporating two N-benzyl substituents are readily mono-debenzylated with CAN or DDQ. An N,N-dibenzyl derivative of a dienylamine with a homoallylic C-N bond is smoothly deblocked by DDQ as well, whereas CAN leads to fragmentation in this case.

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