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Hydroxy-[[N-(4-methylphenyl)sulfonylcarbamimidoyl]amino]-oxo-azanium is a complex organic compound with the chemical formula C9H13N3O4S. It is characterized by the presence of a hydroxy group, a sulfonyl group attached to a 4-methylphenyl ring, and a carbamimidoyl group connected to an amino group. hydroxy-[[N-(4-methylphenyl)sulfonylcarbamimidoyl]amino]-oxo-azanium is a zwitterion, meaning it contains both a positively charged amine group and a negatively charged hydroxy group, which can participate in various chemical reactions and interactions. Due to its unique structure, it has potential applications in the fields of pharmaceuticals, agrochemicals, and materials science, where it may be used as an intermediate in the synthesis of more complex molecules or as a reagent in chemical transformations.

5465-99-6

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5465-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5465-99-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5465-99:
(6*5)+(5*4)+(4*6)+(3*5)+(2*9)+(1*9)=116
116 % 10 = 6
So 5465-99-6 is a valid CAS Registry Number.

5465-99-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N1-tosyl-N2-nitroguanidine

1.2 Other means of identification

Product number -
Other names N1-t-Butyl-N2-phenylpropenamidine

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

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More Details:5465-99-6 SDS

5465-99-6Relevant academic research and scientific papers

SYNTHESIS AND PROPERTIES OF ISOMERIC N-ARYLSULFONYL-N-NITROGUANIDINES

Dobonravov, A. N.,Dubina, V. L.,Svistun, N. V.

, p. 480 - 483 (2007/10/02)

Methods were developed for the synthesis of isomeric N-tosyl-N-nitroguanidines with the nitro group at various nitrogen atoms.Their reactions with diazomethane, acetylacetone, and primary amines and their alkaline hydrolysis were studied.A new method is developed for the production of N1-tosyl-N2-alkylguanidines.

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