Cas 111453-27-1,Benzoyl chloride, 3-[acetyl[2,3-bis(acetyloxy)propyl]amino]-2,4,6-triiodo-5-[(methylamino) carbonyl]-

111453-27-1

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Basic information

Product Name: Benzoyl chloride, 3-[acetyl[2,3-bis(acetyloxy)propyl]amino]-2,4,6-triiodo-5-[(methylamino) carbonyl]-
Synonyms:
CAS NO:111453-27-1
Molecular Formula: C18H18ClI3N2O7
Molecular Weight: 790.517
EINECS: N/A
Product Categories: N/A
Mol File: 111453-27-1.mol

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: Benzoyl chloride, 3-[acetyl[2,3-bis(acetyloxy)propyl]amino]-2,4,6-triiodo-5-[(methylamino) carbonyl]-(CAS DataBase Reference)
NIST Chemistry Reference: Benzoyl chloride, 3-[acetyl[2,3-bis(acetyloxy)propyl]amino]-2,4,6-triiodo-5-[(methylamino) carbonyl]-(111453-27-1)
EPA Substance Registry System: Benzoyl chloride, 3-[acetyl[2,3-bis(acetyloxy)propyl]amino]-2,4,6-triiodo-5-[(methylamino) carbonyl]-(111453-27-1)

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: 111453-27-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 111453-27-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,4,5 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111453-27:
(8*1)+(7*1)+(6*1)+(5*4)+(4*5)+(3*3)+(2*2)+(1*7)=81
81 % 10 = 1
So 111453-27-1 is a valid CAS Registry Number.

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111453-27-1Relevant academic research and scientific papers

Non-ionic polyol contrast media from ionic contrast media

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, (2008/06/13)

Novel non-ionic contrast media of a hitherto unknown combination of low osmolality and low viscosity are efficiently prepared from generally available ionic contrast media or non-iodinated precursors. Particularly, polyhydroxyhalo-hydrocarbons are employed with a triiodo-substituted acylamido benzoic acids in aqueous weakly basic media to selectively substitute the amido nitrogen, followed by activation of the carboxyl group for amide formation.

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