Cas 325776-12-3,25,27-DIMETHOXY-26-(N-TRIFLUOROACETYL)CARBAMOYLOXY-P-TERT-BUTYLCALIX[4!ARENE, 95

325776-12-3

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Basic information

Product Name: 25,27-DIMETHOXY-26-(N-TRIFLUOROACETYL)CARBAMOYLOXY-P-TERT-BUTYLCALIX[4!ARENE, 95
Synonyms: 25,27-DIMETHOXY-26-(N-TRIFLUOROACETYL)CARBAMOYLOXY-P-TERT-BUTYLCALIX[4!ARENE, 95
CAS NO:325776-12-3
Molecular Formula: C49H60F3NO5
Molecular Weight: 800.009
EINECS: N/A
Product Categories: N/A
Mol File: 325776-12-3.mol

Chemical Properties

Melting Point: 230 °C
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 25,27-DIMETHOXY-26-(N-TRIFLUOROACETYL)CARBAMOYLOXY-P-TERT-BUTYLCALIX[4!ARENE, 95(CAS DataBase Reference)
NIST Chemistry Reference: 25,27-DIMETHOXY-26-(N-TRIFLUOROACETYL)CARBAMOYLOXY-P-TERT-BUTYLCALIX[4!ARENE, 95(325776-12-3)
EPA Substance Registry System: 25,27-DIMETHOXY-26-(N-TRIFLUOROACETYL)CARBAMOYLOXY-P-TERT-BUTYLCALIX[4!ARENE, 95(325776-12-3)

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: 325776-12-3(Hazardous Substances Data)

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Chemical Properties

white granular crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 325776-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,5,7,7 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 325776-12:
(8*3)+(7*2)+(6*5)+(5*7)+(4*7)+(3*6)+(2*1)+(1*2)=153
153 % 10 = 3
So 325776-12-3 is a valid CAS Registry Number.

325776-12-3Upstream product

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325776-12-3Relevant academic research and scientific papers

Selective Mono-O-acylation of C2V-symmetrical calix[4]arenediols with acylisocyanates

Yakovenko, Anton V.,Boyko, Vyacheslav I.,Kushnir, Oleg V.,Tsymbal, Ivan F.,Lipkowski, Janusz,Shivanyuk, Alexander,Kalchenko, Vitaly I.

, p. 2769 - 2772 (2007/10/03)

Calix[4]arenedialkyl ethers 3 react with an excess of acylisocyanates to give selectively monoacylated products 4. Intramolecular hydrogen bonds and steric effects of the acylcarbamate fragments are most likely responsible for the high selectivity of this

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