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2-[5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-[5-(succinimidooxycarbonyl)pentyl]-3H-indolium chloride is a complex organic compound characterized by a long carbon chain with multiple double bonds and substituent groups, including an indolium ring and a succinimidooxycarbonyl group. The presence of the chloride ion indicates that the compound is in its salt form. This highly specialized chemical may have applications in various fields such as pharmaceuticals, biochemistry, and material science.

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  • 2-[5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-[5-(succinimidooxycarbonyl)pentyl]-3H-indolium chloride

    Cas No: 1032678-42-4

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  • 1032678-42-4 Structure
  • Basic information

    1. Product Name: 2-[5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-[5-(succinimidooxycarbonyl)pentyl]-3H-indolium chloride
    2. Synonyms: 2-[5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-[5-(succinimidooxycarbonyl)pentyl]-3H-indolium chloride
    3. CAS NO:1032678-42-4
    4. Molecular Formula:
    5. Molecular Weight: 616.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1032678-42-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-[5-(succinimidooxycarbonyl)pentyl]-3H-indolium chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-[5-(succinimidooxycarbonyl)pentyl]-3H-indolium chloride(1032678-42-4)
    11. EPA Substance Registry System: 2-[5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-[5-(succinimidooxycarbonyl)pentyl]-3H-indolium chloride(1032678-42-4)
  • 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: 1032678-42-4(Hazardous Substances Data)

1032678-42-4 Usage

Uses

Used in Pharmaceutical Industry:
2-[5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-[5-(succinimidooxycarbonyl)pentyl]-3H-indolium chloride is used as a bioconjugation agent for protein labeling due to its succinimidooxycarbonyl group, which allows for the attachment of proteins and other biomolecules, facilitating the development of targeted drug delivery systems and diagnostic tools.
Used in Biochemistry Research:
In biochemistry, 2-[5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-[5-(succinimidooxycarbonyl)pentyl]-3H-indolium chloride serves as a versatile reagent for the modification of biomolecules, enabling the study of protein structure, function, and interactions, as well as the development of novel biosensors and imaging agents.
Used in Material Science:
2-[5-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)-1,3-pentadienyl]-3,3-dimethyl-1-[5-(succinimidooxycarbonyl)pentyl]-3H-indolium chloride is utilized in the development of advanced materials with unique properties, such as stimuli-responsive polymers, self-assembling systems, and functional coatings, owing to its complex structure and the presence of multiple reactive sites.

Check Digit Verification of cas no

The CAS Registry Mumber 1032678-42-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,2,6,7 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1032678-42:
(9*1)+(8*0)+(7*3)+(6*2)+(5*6)+(4*7)+(3*8)+(2*4)+(1*2)=134
134 % 10 = 4
So 1032678-42-4 is a valid CAS Registry Number.

1032678-42-4Downstream Products

1032678-42-4Relevant articles and documents

Small Molecule Recognition Triggers Secondary and Tertiary Interactions in DNA Folding and Hammerhead Ribozyme Catalysis

Mao, Jie,Desantis, Chris,Bong, Dennis

supporting information, p. 9815 - 9818 (2017/08/02)

We have identified tris(2-aminoethyl)amine (tren)-derived scaffolds with two (t2M) or four (t4M) melamine rings that can target oligo T/U domains in DNA/RNA. Unstructured T-rich DNAs cooperatively fold with the tren derivatives to form hairpin-like structures. Both t2M and t4M act as functional switches in a family of hammerhead ribozymes deactivated by stem or loop replacement with a U-rich sequence. Catalysis of bond scission in these hammerhead ribozymes could be restored by putative t2M/t4M refolding of stem secondary structure or tertiary bridging interactions between loop and stem. The simplicity of the t2M/t4M binding site enables programming of allostery in RNAs, recoding oligo-U domains as potential sites for secondary structure or tertiary contact. In combination with a facile and general method for installation of the t2M motif on primary amines, the method described herein streamlines design of synthetic allosteric riboswitches and small molecule-nucleic acid complexes.

A convenient synthesis of cyanine dyes: Reagents for the labeling of biomolecules

Kvach, Maksim V.,Ustinov, Alexey V.,Stepanova, Irina A.,Malakhov, Andrei D.,Skorobogatyi, Mikhail V.,Shmanai, Vadim V.,Korshun, Vladimir A.

experimental part, p. 2107 - 2117 (2009/04/05)

Four tetramethylindo(di)carbocyanine-derived carboxylic acids have been prepared using a modified one-pot procedure for the dye assembly. The acids were converted into oxysuccinimide esters and phosphoramidite reagents. The efficiency of the reagents in t

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