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CAS

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198127-92-3

N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE is a chemical compound that is frequently utilized in the realm of organic chemistry. It is composed of nitrogen, sulfur, iodine, carbon, and hydrogen, which gives it a unique chemical structure. N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE is particularly valuable for research and development purposes. However, due to its complexity, it is crucial that it is handled only by professionals and within controlled environments. While its potential hazards or toxicity are not extensively documented, it is imperative to exercise caution when working with N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE. A thorough understanding and knowledge of N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE are essential for its safe and effective use.

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  • 198127-92-3 Structure

  • Basic information

    1. Product Name: N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE
    2. Synonyms: N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE;N,N-Dimethyl 4,5-Diiodo-1H-imidazole-1-sulphonamide;Zinc04352743;4,5-Diiodo-N,N-dimethyl-1H-imidazole-1-sulfonamide;4,5-diiodo-N,N-dimethylimidazole-1-sulfonamide
    3. CAS NO:198127-92-3
    4. Molecular Formula: C5H7I2N3O2S
    5. Molecular Weight: 427
    6. EINECS: N/A
    7. Product Categories: blocks;Imidazoles;Iodides;Sulfonamides
    8. Mol File: 198127-92-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 444.3°Cat760mmHg
    3. Flash Point: 222.5°C
    4. Appearance: /
    5. Density: 2.59g/cm3
    6. Vapor Pressure: 4.34E-08mmHg at 25°C
    7. Refractive Index: 1.774
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE(198127-92-3)
    12. EPA Substance Registry System: N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE(198127-92-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 198127-92-3(Hazardous Substances Data)

198127-92-3 Usage

Uses

Used in Organic Chemistry Research:
N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE is used as a research compound for its unique chemical properties. Its complex structure makes it a valuable tool in the exploration of new chemical reactions and processes.
Used in Pharmaceutical Development:
In the pharmaceutical industry, N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE is used as a potential candidate for drug development. Its chemical composition may contribute to the creation of new medications, particularly in the areas of organic chemistry and medicinal chemistry.
Used in Material Science:
N,N-DIMETHYL 4,5-DIIODO-1H-IMIDAZOLE-1-SULFONAMIDE is employed as a component in the development of new materials. Its unique chemical structure may offer properties that can be harnessed in the creation of advanced materials with specific characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 198127-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,1,2 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 198127-92:
(8*1)+(7*9)+(6*8)+(5*1)+(4*2)+(3*7)+(2*9)+(1*2)=173
173 % 10 = 3
So 198127-92-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H7I2N3O2S/c1-9(2)13(11,12)10-3-8-4(6)5(10)7/h3H,1-2H3

198127-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-diiodo-N,N-dimethylimidazole-1-sulfonamide

1.2 Other means of identification

Product number -
Other names 4,5-diiodo-N,N-dimethyl-1H-imidazole-1-sulfonamide

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:198127-92-3 SDS

198127-92-3Relevant articles and documents

Synthesis and Diels-Alder reactions of 4-vinylimidazoles

Lovely, Carl J.,Du, Hongwang,Dias, H. V. Rasika

, p. 1319 - 1322 (2007/10/03)

(equation presented) The synthesis of several 4-vinylimidazoles via Stille cross-coupling reactions of the corresponding protected 4-iodoimidazoles with tributylvinylstannane is described. These heterocyclic dienes are shown to be effective partners in th

Polyfunctionalisation of imidazole via sequential imidazolyl anion formation

Carver, David S.,Lindell, Stephen D.,Saville-Stones, Elizabeth A.

, p. 14481 - 14496 (2007/10/03)

A method for achieving the sequential functionalisation of the imidazole ring in the order C-5→C-4→C-2 is described. The chemistry proceeds via the regioselective formation of positionally stable imidazolyl anions which are reacted with electrophiles (aldehydes, alkyl halides, azides, formamides, isocyanates) to afford substituted imidazoles in 31-90% yield.

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