Cas 910134-14-4,2-(3,3'''-bis-benzyloxy-2,3'',2'''-tris-diethylcarbamoylmethoxy-3',2''-dihydroxy-[1,1';4',1'';4'',1''']quaternaphthalen-2'-yloxy)-<i>N</i>,<i>N</i>-diethyl-acetamide

910134-14-4

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Basic information

Product Name: 2-(3,3'''-bis-benzyloxy-2,3'',2'''-tris-diethylcarbamoylmethoxy-3',2''-dihydroxy-[1,1';4',1'';4'',1''']quaternaphthalen-2'-yloxy)-N,N-diethyl-acetamide
Synonyms:
CAS NO:910134-14-4
Molecular Formula:
Molecular Weight: 1267.53
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: 2-(3,3'''-bis-benzyloxy-2,3'',2'''-tris-diethylcarbamoylmethoxy-3',2''-dihydroxy-[1,1';4',1'';4'',1''']quaternaphthalen-2'-yloxy)-N,N-diethyl-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3,3'''-bis-benzyloxy-2,3'',2'''-tris-diethylcarbamoylmethoxy-3',2''-dihydroxy-[1,1';4',1'';4'',1''']quaternaphthalen-2'-yloxy)-N,N-diethyl-acetamide(910134-14-4)
EPA Substance Registry System: 2-(3,3'''-bis-benzyloxy-2,3'',2'''-tris-diethylcarbamoylmethoxy-3',2''-dihydroxy-[1,1';4',1'';4'',1''']quaternaphthalen-2'-yloxy)-N,N-diethyl-acetamide(910134-14-4)

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: 910134-14-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 910134-14-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,1,3 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 910134-14:
(8*9)+(7*1)+(6*0)+(5*1)+(4*3)+(3*4)+(2*1)+(1*4)=114
114 % 10 = 4
So 910134-14-4 is a valid CAS Registry Number.

910134-14-4Upstream product

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910134-14-4Relevant academic research and scientific papers

Bottom-up synthesis of optically active oligonaphthalenes: Three different pathways for controlling axial chirality

Tsubaki, Kazunori,Tanaka, Hiroyuki,Takaishi, Kazuto,Miura, Masaya,Morikawa, Hiroshi,Furuta, Takumi,Tanaka, Kiyoshi,Fuji, Kaoru,Sasamori, Takahiro,Tokitoh, Norihiro,Kawabata, Takeo

, p. 6579 - 6587 (2006)

The oxidative homocoupling of optically active binaphthalenes 1a-d with a stoichiometric amount of CuCl2 and amines afforded quaternaphthalenes 2a-d in up to 93% de. The high diastereoselectivities were achieved through three different pathways

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