Cas no 35708-82-8 (N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride)

N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride is a chemically synthesized compound primarily used in pharmaceutical and biochemical research. Its structure features imidodicarbonimidic diamide core functionalized with isopropyl groups, enhancing stability and reactivity. The hydrochloride salt form improves solubility in aqueous and polar organic solvents, facilitating its application in synthetic and analytical processes. This compound serves as a key intermediate in the development of therapeutic agents, particularly in studies involving enzyme inhibition or receptor modulation. Its high purity and well-defined chemical properties make it suitable for precision research applications. Proper handling and storage under controlled conditions are recommended to maintain its integrity.
N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride structure
35708-82-8 structure
Product Name:N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride
CAS No:35708-82-8
MF:C8H20ClN5
MW:221.730899810791
MDL:MFCD27966016
CID:318829
PubChem ID:72941549
Update Time:2025-05-24

N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride Chemical and Physical Properties

Names and Identifiers

    • Proguanil Related Compound D
    • 2-propan-2-yl-1-(N\'-propan-2-ylcarbamimidoyl)guanidine,hydrochloride
    • 2-propan-2-yl-1-(N'-propan-2-ylcarbamimidoyl)guanidine,hydrochloride
    • N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride
    • 1,5-Bis(1-methylethyl)biguanide monohydrochloride
    • 35708-82-8
    • Imidodicarbonimidic diamide, N,N'-bis(1-methylethyl)-, hydrochloride
    • 1,5-Bis-(1-methylethyl)-biguanide hydrochloride
    • EN300-225051
    • UNII-X782QX942G
    • Q27293635
    • AKOS027196608
    • GS-18667
    • X782QX942G
    • 2-propan-2-yl-1-(N'-propan-2-ylcarbamimidoyl)guanidine;hydrochloride
    • N'-(propan-2-yl)-1-[N''-(propan-2-yl)carbamimidamido]methanimidamide hydrochloride
    • Z2216711564
    • 1,5-Bis(1-methylethyl)biguanide hydrochloride
    • Proguanil Related Compound D (25 mg) (1,5-bis(1-methylethyl)biguanide hydrochloride)
    • MDL: MFCD27966016
    • Inchi: 1S/C8H19N5.ClH/c1-5(2)11-7(9)13-8(10)12-6(3)4;/h5-6H,1-4H3,(H5,9,10,11,12,13);1H
    • InChI Key: BKFUVMLPDXIDPQ-UHFFFAOYSA-N
    • SMILES: Cl.N(=C(/N)\N/C(/N)=N/C(C)C)/C(C)C

Computed Properties

  • Exact Mass: 221.14100
  • Monoisotopic Mass: 221.1407234g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 4
  • Complexity: 183
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 88.8?2

Experimental Properties

  • PSA: 83.79000
  • LogP: 2.61570

N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride Security Information

  • Hazardous Material transportation number:NONH for all modes of transport
  • WGK Germany:3

N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride Pricemore >>

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N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride Related Literature

Additional information on N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride

Comprehensive Overview of N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride (CAS No. 35708-82-8)

N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride (CAS No. 35708-82-8) is a specialized chemical compound widely recognized in pharmaceutical and biochemical research. This compound, often referred to by its systematic name, plays a critical role in the synthesis of advanced imidodicarbonimidic diamide derivatives. Its unique molecular structure, featuring isopropyl groups and a hydrochloride salt, makes it a valuable intermediate in the development of novel therapeutic agents and bioactive molecules.

In recent years, the demand for N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride has surged due to its applications in drug discovery and medicinal chemistry. Researchers are particularly interested in its potential to modulate enzyme activity and protein interactions, which are hot topics in the field of precision medicine. The compound's ability to act as a building block for more complex structures has also made it a focal point in combinatorial chemistry and high-throughput screening.

One of the most frequently asked questions about CAS No. 35708-82-8 is its stability and solubility profile. Studies indicate that the hydrochloride salt form enhances its solubility in aqueous solutions, making it suitable for in vitro and in vivo studies. This property is particularly advantageous for researchers working on biocompatible materials and drug delivery systems, which are currently trending in biomedical engineering.

The synthesis of N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride involves a series of organic reactions, including condensation and salt formation. These processes are optimized to ensure high purity and yield, which are critical for pharmaceutical-grade applications. The compound's spectroscopic data (e.g., NMR, IR) and chromatographic profiles are well-documented, providing researchers with reliable references for quality control.

Another area of interest is the compound's role in green chemistry. With growing emphasis on sustainable synthesis, researchers are exploring eco-friendly methods to produce imidodicarbonimidic diamide derivatives. This aligns with global trends in environmentally friendly chemical production, a topic frequently searched in academic databases and industry forums.

In summary, N,N'-Bis(1-methylethyl)Imidodicarbonimidic Diamide Hydrochloride (CAS No. 35708-82-8) is a versatile compound with significant applications in pharmaceutical research, biotechnology, and material science. Its unique properties and growing relevance in cutting-edge research make it a subject of ongoing investigation and innovation.

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