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N-METHYLHYDRAZINECARBOXIMIDAMIDEHYDROIODIDE, also known as 1-Methyl-3-aminoguanidine Hydriodide, is a chemical compound with the molecular formula C2H7N4I. It is a white crystalline solid that is soluble in water and has a role as a reactant in the synthesis of heterocyclic aldehydes.

33398-79-7

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33398-79-7 Usage

Uses

Used in Chemical Synthesis:
N-METHYLHYDRAZINECARBOXIMIDAMIDEHYDROIODIDE is used as a reactant for the preparation of heterocyclic aldehydes. It serves as a key intermediate in the synthesis of various complex organic molecules, particularly those with heterocyclic structures.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-METHYLHYDRAZINECARBOXIMIDAMIDEHYDROIODIDE may be utilized as a building block for the development of new drugs, particularly those targeting specific biological pathways or receptors. Its unique chemical structure allows for the creation of novel compounds with potential therapeutic applications.
Used in Research and Development:
N-METHYLHYDRAZINECARBOXIMIDAMIDEHYDROIODIDE is also used in research and development settings, where it can be employed to study the properties and reactivity of heterocyclic compounds. This can lead to a better understanding of their potential applications in various fields, including medicine, materials science, and environmental science.

Check Digit Verification of cas no

The CAS Registry Mumber 33398-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,3,9 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33398-79:
(7*3)+(6*3)+(5*3)+(4*9)+(3*8)+(2*7)+(1*9)=137
137 % 10 = 7
So 33398-79-7 is a valid CAS Registry Number.

33398-79-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-amino-2-methylguanidine,hydroiodide

1.2 Other means of identification

Product number -
Other names N-Methylhydrazinecarboximidamide hydroiodide

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:33398-79-7 SDS

33398-79-7Relevant academic research and scientific papers

NOVEL 5-HT2 ANTAGONISTS

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Paragraph 0110, (2017/01/05)

The present invention relates to 1-amidino-3-aryl-2-pyrazoline derivatives of the general formula I The invention specifically relates to such derivatives which exhibit antagonizing activity towards serotonin 5-HT2B receptors. The present invention also relates to use of said compounds as a medicament and for the treatment of fibrosis, cardiovascular diseases, pain, IBD, and other inflammatory diseases, as well as pharmaceutical compositions comprising one or more of said compounds and methods of treatment.

Synthesis and biological activity of guanylhydrazones of 2- and 4-pyridine and 4-quinoline carboxaldehydes

Foye,Almassian,Eisenberg,Maher

, p. 527 - 530 (2007/10/02)

A series of guanylhydrazones derived from 2- and 4-pyridine and 4-quinoline carboxaldehydes was synthesized from S-methylisothiosemicarbazide hydroiodide using known procedures. The compounds are analogous to anticancer and antiviral thiosemicarbazones, b

Cationic Antiprotozoal Drugs. Trypanocidal Activity of 2-(4'-Formylphenyl)imidazopyridinium Guanylhydrazones and Related Derivatives of Quaternary Heteroaromatic Compounds

Sundberg, Richard J.,Dahlhausen, Daniel J.,Manikumar, G.,Mavunkel, B.,Biswas, A.,et al.

, p. 298 - 307 (2007/10/02)

A series of quaternary 2-phenylimidazopyridinium salts has been prepared and evaluated for antiparasitic activity.Primary attention was focused on derivatives with amido, substituted hydrazone, and heterocyclic functionality at the para position of

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