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4-MaleiMidobutyric Acid Hydrazide Trifluoroacetate is a maleimide derivative characterized by its unique chemical structure and properties. It is a compound that has found applications in various fields due to its reactivity and functional groups.

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  • 1239587-68-8 Structure
  • Basic information

    1. Product Name: 4-MaleiMidobutyric Acid Hydrazide Trifluoroacetate
    2. Synonyms: 4-MaleiMidobutyric Acid Hydrazide Trifluoroacetate;2,5-Dihydro-2,5-dioxo-1H-Pyrrole-1-butanoic Acid Hydrazide 2,2,2-Trifluoroacetate;4-MaleiMidobutyric acid hydrazide trifluoroacetic acid salt
    3. CAS NO:1239587-68-8
    4. Molecular Formula: C10H12F3N3O5
    5. Molecular Weight: 311.2145896
    6. EINECS: N/A
    7. Product Categories: Heterocycles;Intermediates;Maleimide Derivatives;MTS & Sulfhydryl Active Reagents
    8. Mol File: 1239587-68-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-MaleiMidobutyric Acid Hydrazide Trifluoroacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-MaleiMidobutyric Acid Hydrazide Trifluoroacetate(1239587-68-8)
    11. EPA Substance Registry System: 4-MaleiMidobutyric Acid Hydrazide Trifluoroacetate(1239587-68-8)
  • 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: 1239587-68-8(Hazardous Substances Data)

1239587-68-8 Usage

Uses

Used in Biochemical Research:
4-MaleiMidobutyric Acid Hydrazide Trifluoroacetate is used as a reagent for the preparation of immunoenzymic conjugates. Its maleimide group allows for selective and efficient conjugation with thiol-containing biomolecules, such as antibodies or enzymes, which is crucial in the development of immunoassays and other diagnostic tools.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-MaleiMidobutyric Acid Hydrazide Trifluoroacetate is utilized as a building block for the synthesis of various drug candidates. Its maleimide functionality can be exploited to create novel compounds with potential therapeutic applications.
Used in Chemical Synthesis:
4-MaleiMidobutyric Acid Hydrazide Trifluoroacetate is also used as an intermediate in the synthesis of complex organic molecules. Its reactive maleimide group can be employed in various chemical reactions, such as Michael additions or thiol-ene reactions, to construct diverse molecular architectures.

Check Digit Verification of cas no

The CAS Registry Mumber 1239587-68-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,9,5,8 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1239587-68:
(9*1)+(8*2)+(7*3)+(6*9)+(5*5)+(4*8)+(3*7)+(2*6)+(1*8)=198
198 % 10 = 8
So 1239587-68-8 is a valid CAS Registry Number.

1239587-68-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2,5-dioxopyrrol-1-yl)butanehydrazide,2,2,2-trifluoroacetic acid

1.2 Other means of identification

Product number -
Other names 4-Maleimidobutyric acid hydrazide trifluoroacetic acid salt

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:1239587-68-8 SDS

1239587-68-8Downstream Products

1239587-68-8Relevant articles and documents

CYTOTOXIC-DRUG DELIVERING MOLECULES TARGETING HIV (CDM-HS), CYTOTOXIC ACTIVITY AGAINST THE HUMAN IMMUNODEFICIENCY VIRUS AND METHODS OF USE

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, (2013/11/18)

The present invention is directed to new bifunctional compounds and methods for treating HIV infections. The bifunctional small molecules, generally referred to as CDM-Hs, function through orthogonal pathways, by inhibiting the gp120-CD4 interaction, and by introducing cytotoxic moieties to gp120-expressing cells, thereby causing cell death and preventing cell infection and spread of HIV. It is shown that CDM-Hs bind to gp120 and gp-120 expressing cells competitively with CD4, and these compounds cause cell death of HIV-infected cells, thereby decreasing viral infectivity. Compounds and methods are described herein.

NOVEL BENZODIAZEPINE DERIVATIVES

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Page/Page column 168, (2010/08/18)

The invention relates to novel benzodiazepine derivatives with antiproliferative activity and more specifically to novel benzodiazepines of formula (I) and (II), in which the diazepine ring (B) is fused with a heterocyclic ring (CD), wherein the heterocyclic ring is bicyclic or a compound of formula (III), in which the diazepine ring (B) is fused with a heterocyclic ring (C), wherein the heterocyclic ring is monocyclic. The invention provides cytotoxic dimers of these compounds. The invention also provides conjugates of the monomers and the dimers. The invention further provides compositions and methods useful for inhibiting abnormal cell growth or treating a proliferative disorder in a mammal using the compounds or conjugates of the invention. The invention further relates to methods of using the compounds or conjugates for in vitro, in situ, and in vivo diagnosis or treatment of mammalian cells, or associated pathological conditions.

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