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.alpha.-D-gluco-Hexodialdo-1,5-pyranoside, 3-deoxy-1-C-(diaminomethoxy)-3-(2-hydroxyethyl)(hydroxymethyl)amino-1-O-methyl-.beta.-D-fructofuranosyl 2-deoxy-2-(2-hydroxyethyl)(hydroxymethyl)amino-, diaminomethyl methyl acetal is a complex organic compound with a unique structure that incorporates elements of glucose and fructose, as well as various functional groups such as hydroxyl, amino, and methyl acetal. .alpha.-D-gluco-Hexodialdo-1,5-pyranoside, 3-deoxy-1-C-(diaminomethoxy)-3-(2-hydroxyethyl)(hydroxymethyl)amino-1-O-methyl-.beta.-D-fructofuranosyl 2-deoxy-2-(2-hydroxyethyl)(hydroxymethyl)amino-, diaminomethyl methyl acetal is significant in the fields of carbohydrate chemistry, biochemistry, and pharmaceuticals due to its potential applications and interactions with biological systems.

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  • .alpha.-D-gluco-Hexodialdo-1,5-pyranoside, 3-deoxy-1-C-(diaminomethoxy)-3-(2-hydroxyethyl)(hydroxymethyl)amino-1-O-methyl-.beta.-D-fructofuranosyl 2-deoxy-2-(2-hydroxyethyl)(hydroxymethyl)amino-, diam

    Cas No: 145033-68-7

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  • 145033-68-7 Structure
  • Basic information

    1. Product Name: .alpha.-D-gluco-Hexodialdo-1,5-pyranoside, 3-deoxy-1-C-(diaminomethoxy)-3-(2-hydroxyethyl)(hydroxymethyl)amino-1-O-methyl-.beta.-D-fructofuranosyl 2-deoxy-2-(2-hydroxyethyl)(hydroxymethyl)amino-, diaminomethyl methyl acetal
    2. Synonyms: .alpha.-D-gluco-Hexodialdo-1,5-pyranoside, 3-deoxy-1-C-(diaminomethoxy)-3-(2-hydroxyethyl)(hydroxymethyl)amino-1-O-methyl-.beta.-D-fructofuranosyl 2-deoxy-2-(2-hydroxyethyl)(hydroxymethyl)amino-, diaminomethyl methyl acetal
    3. CAS NO:145033-68-7
    4. Molecular Formula: C22H48 N6 O15
    5. Molecular Weight: 636.65
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 145033-68-7.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: .alpha.-D-gluco-Hexodialdo-1,5-pyranoside, 3-deoxy-1-C-(diaminomethoxy)-3-(2-hydroxyethyl)(hydroxymethyl)amino-1-O-methyl-.beta.-D-fructofuranosyl 2-deoxy-2-(2-hydroxyethyl)(hydroxymethyl)amino-, diaminomethyl methyl acetal(CAS DataBase Reference)
    10. NIST Chemistry Reference: .alpha.-D-gluco-Hexodialdo-1,5-pyranoside, 3-deoxy-1-C-(diaminomethoxy)-3-(2-hydroxyethyl)(hydroxymethyl)amino-1-O-methyl-.beta.-D-fructofuranosyl 2-deoxy-2-(2-hydroxyethyl)(hydroxymethyl)amino-, diaminomethyl methyl acetal(145033-68-7)
    11. EPA Substance Registry System: .alpha.-D-gluco-Hexodialdo-1,5-pyranoside, 3-deoxy-1-C-(diaminomethoxy)-3-(2-hydroxyethyl)(hydroxymethyl)amino-1-O-methyl-.beta.-D-fructofuranosyl 2-deoxy-2-(2-hydroxyethyl)(hydroxymethyl)amino-, diaminomethyl methyl acetal(145033-68-7)
  • 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: 145033-68-7(Hazardous Substances Data)

145033-68-7 Usage

Uses

Used in Carbohydrate Chemistry Research:
.alpha.-D-gluco-Hexodialdo-1,5-pyranoside, 3-deoxy-1-C-(diaminomethoxy)-3-(2-hydroxyethyl)(hydroxymethyl)amino-1-O-methyl-.beta.-D-fructofuranosyl 2-deoxy-2-(2-hydroxyethyl)(hydroxymethyl)amino-, diaminomethyl methyl acetal is used as a research compound for studying the properties and interactions of complex carbohydrates. Its unique structure allows scientists to explore various aspects of carbohydrate chemistry, including glycosidic linkages, conformational analysis, and the role of functional groups in molecular recognition.
Used in Biochemical Applications:
In the field of biochemistry, .alpha.-D-gluco-Hexodialdo-1,5-pyranoside, 3-deoxy-1-C-(diaminomethoxy)-3-(2-hydroxyethyl)(hydroxymethyl)amino-1-O-methyl-.beta.-D-fructofuranosyl 2-deoxy-2-(2-hydroxyethyl)(hydroxymethyl)amino-, diaminomethyl methyl acetal can be employed as a tool to investigate the role of carbohydrates in biological processes. Its complex structure may help researchers understand the mechanisms of carbohydrate metabolism, enzyme interactions, and the role of carbohydrates in cellular signaling.
Used in Pharmaceutical Development:
.alpha.-D-gluco-Hexodialdo-1,5-pyranoside, 3-deoxy-1-C-(diaminomethoxy)-3-(2-hydroxyethyl)(hydroxymethyl)amino-1-O-methyl-.beta.-D-fructofuranosyl 2-deoxy-2-(2-hydroxyethyl)(hydroxymethyl)amino-, diaminomethyl methyl acetal has potential applications in the pharmaceutical industry, particularly in the development of novel drugs targeting carbohydrate-related diseases. Its unique structure and functional groups may be exploited to design drugs that can modulate carbohydrate metabolism, inhibit specific enzymes, or interact with cellular receptors involved in various pathological conditions.
Used in Drug Delivery Systems:
In the context of drug delivery, .alpha.-D-gluco-Hexodialdo-1,5-pyranoside, 3-deoxy-1-C-(diaminomethoxy)-3-(2-hydroxyethyl)(hydroxymethyl)amino-1-O-methyl-.beta.-D-fructofuranosyl 2-deoxy-2-(2-hydroxyethyl)(hydroxymethyl)amino-, diaminomethyl methyl acetal may be utilized as a component in the design of targeted drug delivery systems. Its complex structure and functional groups could be used to develop carriers that can selectively deliver therapeutic agents to specific cells or tissues, thereby improving the efficacy and reducing the side effects of certain treatments.
Used in Diagnostic Applications:
.alpha.-D-gluco-Hexodialdo-1,5-pyranoside, 3-deoxy-1-C-(diaminomethoxy)-3-(2-hydroxyethyl)(hydroxymethyl)amino-1-O-methyl-.beta.-D-fructofuranosyl 2-deoxy-2-(2-hydroxyethyl)(hydroxymethyl)amino-, diaminomethyl methyl acetal may also find use in the development of diagnostic tools and assays. Its unique structure could be employed to create probes or markers that can specifically recognize and bind to target molecules, allowing for the detection and quantification of various biological processes or conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 145033-68-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,0,3 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 145033-68:
(8*1)+(7*4)+(6*5)+(5*0)+(4*3)+(3*3)+(2*6)+(1*8)=107
107 % 10 = 7
So 145033-68-7 is a valid CAS Registry Number.

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