Cas 868635-48-7,1-(anthracen-9-ylmethoxy)-3-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-propan-2-ol

868635-48-7

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Basic information

Product Name: 1-(anthracen-9-ylmethoxy)-3-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-propan-2-ol
Synonyms: 1-(anthracen-9-ylmethoxy)-3-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-propan-2-ol
CAS NO:868635-48-7
Molecular Formula:
Molecular Weight: 584.712
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: 1-(anthracen-9-ylmethoxy)-3-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-propan-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: 1-(anthracen-9-ylmethoxy)-3-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-propan-2-ol(868635-48-7)
EPA Substance Registry System: 1-(anthracen-9-ylmethoxy)-3-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-propan-2-ol(868635-48-7)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 868635-48-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 868635-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,6,3 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 868635-48:
(8*8)+(7*6)+(6*8)+(5*6)+(4*3)+(3*5)+(2*4)+(1*8)=227
227 % 10 = 7
So 868635-48-7 is a valid CAS Registry Number.

868635-48-7Upstream product

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868635-48-7Relevant academic research and scientific papers

Enhanced reactivity of amino-modified oligonucleotides by insertion of aromatic residue

Kojima, Naoshi,Sugino, Maiko,Mikami, Akiko,Nonaka, Ken,Fujinawa, Yumi,Muto, Isamu,Matsubara, Kenichi,Ohtsuka, Eiko,Komatsu, Yasuo

, p. 5118 - 5121 (2006)

We developed novel amino-modifying reagents, of which an amino group was connected with an aromatic residue by aliphatic linker. It was proved that the insertion of the aromatic residue could increase the reactivity of the amino group on oligonucleotides

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