mannono-1,5-lactone

Base Information

• Chemical Name: mannono-1,5-lactone
• CAS No.: 10366-75-3
• Molecular Formula: C₆H₁₀O₆
• Molecular Weight: 178.142
• Mol file: 10366-75-3.mol

Synonyms:mannono-1,5-lactone

Chemical Property of mannono-1,5-lactone

Chemical Property:

• Vapor Pressure: 7.6E-10mmHg at 25°C
• Refractive Index: 1.607
• Boiling Point: 446.4°Cat760mmHg
• PKA: 12.13±0.70(Predicted)
• Flash Point: 192.3°C
• PSA: 107.22000
• Density: 1.72g/cm³
• LogP: -3.01320

Purity/Quality:

98%,99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Use Description: (1E)-4-carboxy-1-[(4-nitrophenyl)imino]-1,2-dihydropyridinium is a chemical compound with various applications in different fields. In the field of organic chemistry and pharmaceutical research, it can serve as a valuable intermediate for the synthesis of complex organic molecules, including potential drug candidates. Its unique structure and functional groups make it valuable in the development of pharmaceuticals targeting various medical conditions. In analytical chemistry, this compound may be employed as a reagent or marker in chemical analysis techniques, contributing to the detection and quantification of specific compounds or reactions. However, the specific role and significance of (1E)-4-carboxy-1-[(4-nitrophenyl)imino]-1,2-dihydropyridinium may vary depending on the particular research or industrial needs within each field, highlighting its potential versatility and importance in diverse scientific endeavors.

Technology Process of mannono-1,5-lactone

There total 1 articles about mannono-1,5-lactone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

L-allonic acid (740753-96-2) → L-allonic acid-5-lactone (90-80-2,7506-65-2,10366-75-3,15892-28-1,32746-79-5,52153-09-0,52393-78-9,110115-45-2,120523-34-4,124819-01-8,124915-65-7,1335-57-5,4253-68-3)

Guidance literature:

With ethanol; schnelles Eindampfen unter vermindertem Druck und Behandeln des Rueckstands mit wasserfreiem Aethanol;

Reference yield:

L-allonic acid-5-lactone (90-80-2,7506-65-2,10366-75-3,15892-28-1,32746-79-5,52153-09-0,52393-78-9,110115-45-2,120523-34-4,124819-01-8,124915-65-7,1335-57-5,4253-68-3) → L-mannonic γ-lactone (78184-43-7)

Guidance literature:

at 130 ℃;

upstream raw materials:

L-allonic acid

Downstream raw materials:

L-mannonic γ-lactone