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4-Amino-2,2,5,5-tetramethyl-2,5-dihydro-1H-imidazol-1-ol 3-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91575-47-2

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91575-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91575-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,7 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 91575-47:
(7*9)+(6*1)+(5*5)+(4*7)+(3*5)+(2*4)+(1*7)=152
152 % 10 = 2
So 91575-47-2 is a valid CAS Registry Number.

91575-47-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dihydroxy-2,2,5,5-tetramethylimidazolidin-4-imine

1.2 Other means of identification

Product number -
Other names 4-amino-2,2,5,5-tetramethyl-3-imidazoline 3,1-dioxide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:91575-47-2 SDS

91575-47-2Downstream Products

91575-47-2Relevant academic research and scientific papers

NMR SPECTRA OF CYCLIC NITRONES. 5 . 13C NMR SPECTRA OF THE POTENTIAL TAUTOMERIC SYSTEMS OF AMINO-, HYDROXY-, AND MERCAPTONITRONES IN THE SERIES OF 3-IMIDAZOLINE 3-OXIDE

Shchukin, G. I.,Girgor'ev, I. A.,Volodarskii, L. B.

, p. 409 - 414 (1990)

The position of the tautomeric equilibrium in amino-, hydroxy-, and mercaptonitrones was determined by the 13C NMR method for the case of the derivatives of 3-imidazoline-3-oxide.It was shown that the tautomeric equilibrium in the OH and SH derivatives is shifted toward the oxo and thioxo forms (ca. 95percent).The chemical shifts of the carbon atoms of the nitrone group in the α-N-, α-O-, and α-S-substituted nitrones lie in the region of 137 - 150 ppm.

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