Cas 775326-39-1,4-[tris(4'-tert-butylphenyl)methyl]phenyl carbamic acid 4-nitrophenyl ester

775326-39-1

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Basic information

Product Name: 4-[tris(4'-tert-butylphenyl)methyl]phenyl carbamic acid 4-nitrophenyl ester
Synonyms: 4-[tris(4'-tert-butylphenyl)methyl]phenyl carbamic acid 4-nitrophenyl ester
CAS NO:775326-39-1
Molecular Formula:
Molecular Weight: 668.876
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: 4-[tris(4'-tert-butylphenyl)methyl]phenyl carbamic acid 4-nitrophenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-[tris(4'-tert-butylphenyl)methyl]phenyl carbamic acid 4-nitrophenyl ester(775326-39-1)
EPA Substance Registry System: 4-[tris(4'-tert-butylphenyl)methyl]phenyl carbamic acid 4-nitrophenyl ester(775326-39-1)

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: 775326-39-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 775326-39-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,5,3,2 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 775326-39:
(8*7)+(7*7)+(6*5)+(5*3)+(4*2)+(3*6)+(2*3)+(1*9)=191
191 % 10 = 1
So 775326-39-1 is a valid CAS Registry Number.

775326-39-1Upstream product

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775326-39-1Relevant academic research and scientific papers

Enhanced thermodynamic and kinetic stability of calix[4]arene dimers locked in the cone conformation

Vysotsky, Myroslav O.,Mogck, Oliver,Rudzevich, Yuliya,Shivanyuk, Alexander,Boehmer, Volker,Brody, Marcus S.,Cho, Young Lag,Rudkevich, Dmitry M.,Rebek Jr., Julius

, p. 6115 - 6120 (2004)

Wide rim tetraurea derivatives (2a,b) have been prepared from a calix[4]arene rigidified in the cone conformation by two diethyleneglycol ether bridges between adjacent oxygens. In comparison to the analogous tetraurea derivatives (3a,b) of a tetrapentoxy

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