Cas 85601-78-1,1-(3-Chloro-phenyl)-3-(4-hydroxyamino-3,5,5-trimethyl-2-oxo-imidazolidin-1-yl)-urea

85601-78-1

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Basic information

Product Name: 1-(3-Chloro-phenyl)-3-(4-hydroxyamino-3,5,5-trimethyl-2-oxo-imidazolidin-1-yl)-urea
Synonyms: 1-(3-Chloro-phenyl)-3-(4-hydroxyamino-3,5,5-trimethyl-2-oxo-imidazolidin-1-yl)-urea
CAS NO:85601-78-1
Molecular Formula:
Molecular Weight: 327.771
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: 1-(3-Chloro-phenyl)-3-(4-hydroxyamino-3,5,5-trimethyl-2-oxo-imidazolidin-1-yl)-urea(CAS DataBase Reference)
NIST Chemistry Reference: 1-(3-Chloro-phenyl)-3-(4-hydroxyamino-3,5,5-trimethyl-2-oxo-imidazolidin-1-yl)-urea(85601-78-1)
EPA Substance Registry System: 1-(3-Chloro-phenyl)-3-(4-hydroxyamino-3,5,5-trimethyl-2-oxo-imidazolidin-1-yl)-urea(85601-78-1)

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: 85601-78-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85601-78-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,0 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85601-78:
(7*8)+(6*5)+(5*6)+(4*0)+(3*1)+(2*7)+(1*8)=141
141 % 10 = 1
So 85601-78-1 is a valid CAS Registry Number.

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85601-78-1Relevant academic research and scientific papers

Synthesis of Acyl Derivatives of α-Hydrazino Oximes and 2-Imidazolidinones Based on Them

Epshtein, S. P.,Rukasov, A. F.,Tashchi, V. P.,Putsykin, Yu. G.,Baskakov, Yu. A.,Simonova, T. G.

, p. 74 - 78 (2007/10/02)

The reaction of N(1)- or N(2)-monoacyl derivatives of 2-hydrazinocyclohexanone, 3-hydrazino-3-methyl-2-butanone, and 2-hydrazino-2-methylpropanal oximes with isocyanates was used to synthesize, N,N-diacyl derivatives, which, under the influence of acids o

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