Recommended Products
Quality Level
form
powder
mp
110-114 °C
storage temp.
2-30°C
InChI
1S/C6H10BO6.Na/c1-4(8)11-7(12-5(2)9)13-6(3)10;/h7H,1-3H3;/q-1;+1
InChI key
HHYFEYBWNZJVFQ-UHFFFAOYSA-N
Related Categories
Application
- Chemical Synthesis: Used in the synthesis of (Piperazine-yl) Methanone derivatives with potential anticancer and antituberculosis activities, highlighting its role in facilitating N-alkylation reactions (Mallikarjuna et al., 2014).
- Green Chemistry: Featured in the development of efficient N-methylation of secondary amines under solvent-free conditions, demonstrating its utility in sustainable chemical processes (Walter et al., 2024).
- Organic Chemistry: Utilized in N-alkylation using carboxylic acids as alkyl sources, providing a versatile method for producing complex organic molecules (Tamura et al., 2018).
Analysis Note
Assay (by gasvolumetry): ≥ 96.0 %
Identity (IR): passes test
Identity (IR): passes test
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Sol. 1 - Repr. 1B - Water-react 1
Supplementary Hazards
Storage Class Code
4.3 - Hazardous materials, which set free flammable gases upon contact with water
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
新产品
Certificates of Analysis (COA)
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Paraconiothins A-J: Sesquiterpenoids from the Endophytic Fungus Paraconiothyrium brasiliense ECN258.
Ken-Ichi Nakashima et al.
Journal of natural products, 82(12), 3347-3356 (2019-12-10)
Paraconiothins A-J (1-10), 10 new sesquiterpenoids, as well as five known sesquiterpenoids, were isolated from the cultures of the endophytic fungus Paraconiothyrium brasiliense ECN-258. The structures of the sesquiterpenoids were elucidated by extensive spectroscopic analysis. Furthermore, the absolute structures of
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