Cas 835874-99-2,5-tert-butyl-N,N'-bis-[3-[2-[2-[(2-nicotinoyloxy)ethoxy]ethoxy]ethoxy]phenyl]-1,3-benzenediamide

835874-99-2

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Basic information

Product Name: 5-tert-butyl-N,N'-bis-[3-[2-[2-[(2-nicotinoyloxy)ethoxy]ethoxy]ethoxy]phenyl]-1,3-benzenediamide
Synonyms: 5-tert-butyl-N,N'-bis-[3-[2-[2-[(2-nicotinoyloxy)ethoxy]ethoxy]ethoxy]phenyl]-1,3-benzenediamide
CAS NO:835874-99-2
Molecular Formula:
Molecular Weight: 878.976
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: 5-tert-butyl-N,N'-bis-[3-[2-[2-[(2-nicotinoyloxy)ethoxy]ethoxy]ethoxy]phenyl]-1,3-benzenediamide(CAS DataBase Reference)
NIST Chemistry Reference: 5-tert-butyl-N,N'-bis-[3-[2-[2-[(2-nicotinoyloxy)ethoxy]ethoxy]ethoxy]phenyl]-1,3-benzenediamide(835874-99-2)
EPA Substance Registry System: 5-tert-butyl-N,N'-bis-[3-[2-[2-[(2-nicotinoyloxy)ethoxy]ethoxy]ethoxy]phenyl]-1,3-benzenediamide(835874-99-2)

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: 835874-99-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 835874-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,5,8,7 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 835874-99:
(8*8)+(7*3)+(6*5)+(5*8)+(4*7)+(3*4)+(2*9)+(1*9)=222
222 % 10 = 2
So 835874-99-2 is a valid CAS Registry Number.

835874-99-2Upstream product

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835874-99-2Relevant academic research and scientific papers

Amide-appended porphyrins as scaffolds for catenanes, rotaxanes and anion receptors

Gunter, Maxwell J.,Farquhar, Sandra M.,Mullen, Kathleen M.

, p. 1443 - 1449 (2007/10/03)

The synthesis of a porphyrin with an over-arching strap incorporating an isophthalamide unit produced both a porphyrin monomer with a potentially H-bonding receptor site, and a [2]catenane. Although both compounds exhibit fluxional behaviour, 1

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