Cesium fluoride - UltraBio™, ≥99%(F) , CAS No.13400-13-0

CAS: 13400-13-0 Cat. No.: C755570 Fórmula: CsF Peso molecular: 151.9 Número CE: 236-487-3
Disponível para encomenda
GRAU & PUREZA UltraBio™ ? UltraBio™ — Aladdin's line for molecular-biology applications. Use for nuclease-free, high-consistency reagents across molecular workflows. ≥99%(F)
Storage
Room temperature
Shipped In
FedEx DG Service
★
Tamanho
USA
Alemanha (EU)*
Preço
Qtd
10g
C755570-10g
Sob encomenda · 8–12 semanas
178,90US$
250g
C755570-250g
Sob encomenda · 8–12 semanas
2334,90US$
Enter a quantity for the sizes you want to add.

Visão geral

Reactant for:
  • Preparation of building blocks for synthesis of fluoroallylic compounds
  • Synthesis of alcohols via hydrolysis of alkyl silyl ethers at neutral pH in buffered mixed organic-aqueous solutions
  • Nucleophilic fluorination of alkynyliodonium salts to form fluorovinylic compounds
  • Nucleophilic aromatic substitution (SNAr) reactions
Used in the successful synthesis of a single-crystal Dion-Jacobson phase, CsLaTa2O7, that has applications in photocatalysis and superconductivity.

Especificações

Especificações e pureza
UltraBio™, ≥99%(F)
Condições de armazenamento de armazenamento
Room temperature
Enviado em
FedEx DG Service
Grau
UltraBio™
Pureza
≥99%(F)
Nomes e identificadores
PH
6.5-7.5 (25 °C, 3 M in H 2 O)
Sorrisos canónicos
[F-].[Cs+]
IUPAC Name
cesium;fluoride
InChIKey
XJHCXCQVJFPJIK-UHFFFAOYSA-M
INCHI
1S/Cs.FH/h;1H/q+1;/p-1
SMILES isoméricas
[F-].[Cs+]
WGK Alemanha
3
RTECS
FK9650000
Número UN
3288
Grupo de embalagem
III
Peso molecular
151.9
Reaxy-Rn
6184400

Dados avançados

Taxonomic Classification

Taxonomy Tree

KingdomInorganic compounds
SuperclassMixed metal/non-metal compounds
ClasseAlkali metal salts
SubclassAlkali metal fluorides
Intermediate Tree Nodes Not available
Direct ParentAlkali metal fluorides
Alternative Parents Inorganic salts  
Molecular FrameworkNot available
Substituents Alkali metal fluoride - Inorganic salt
DescriçãoThis compound belongs to the class of inorganic compounds known as alkali metal fluorides. These are inorganic compounds in which the largest halogen atom is fluorine, and the heaviest metal atom is an alkali metal.
External Descriptors Not available
Estrutura 3D
Modelo de Estrutura Química Interativa





Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propriedades químicas e físicas
SolubilidadeH 2 O: 3 M at 20 °C, clear, colorless
Ponto de ebulição (°C)1251°C
Ponto de fusão (°C)682 °C
Peso molecular151.903 g/mol
XLogP3
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass151.904 Da
Monoisotopic Mass151.904 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count2
Formal Charge0
Complexity2.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count2
FAQs e artigos
UltraBio™: Defining Excellence in Molecular Biology Applications
One Atom Can Change a Drug’s Fate: Atom-Level Knobs and a Functional-Group Toolbox for Medicinal Chemistry (Methyl / Halogen Bonding / 3D Building Blocks / Late-Stage Fluorination + Product-Selection Tables)
Late-Stage Fluorination Toolbox: “Minimally Invasive Upgrades” for Lead Candidates: Four “Fluorine Knobs” → Two major routes (electrophilic vs nucleophilic) → An ¹⁸F-PET tracer branch → Selection navigation & representative product list
OSF/ASF Dual-Channel Toolbox: Divergent Reactions of Four-Membered Ring Sulfonyl Fluorides, Condition “Knobs,” and Selection Navigation
Selection of Common Research Salts: A Task Map for Alkali Metal Salts & Alkaline Earth Metal Salts (with Product Tables 1–6)
Perovskite PV/PeLED Precursor Guide: Selecting Metal Halide Salts, Key Conditions, and Reproducible Performance (including Product Tables 1–4 and a Selection Navigation Guide)
How to Make the Suzuki–Miyaura Reaction Robust: Pinpoint the Bottleneck and Lock in a Reproducible Operating Window (with Selection Navigation and Product Tables 1–5)
Silicon Reagent-Assisted Peptide Synthesis: Research Progress and Methodological Value of Peptide Bond Formation from Unprotected Substrates
TMSE, Teoc, and SEM: Functional Roles and Selection Logic of Three 2-(Trimethylsilyl)ethyl-Derived Protecting Systems
Selection Logic for the Teoc Amino Protecting Group: From Fluoride-Triggered Deprotection to Orthogonal Protecting-Group Design
Experimental Selection of SEM-Cl: From O/N-SEM Protection and Directed Functionalization of N-Heterocycles to the Introduction of Protected C1 Fragments
4-[(tert-Butyldimethylsilyl)oxy]butan-1-ol: Experimental Selection Logic as a Monoprotected 1,4-Butanediol Building Block and a Protected C4 Linker
Design Logic of Fluorinated 3,3-Disubstituted Oxetane Building Blocks: Structural Construction and Modulation of Amine Basicity, Lipophilicity, and Metabolic Stability
Selectivity Mechanism of the Triple Aryne–Tetrazine Cascade Reaction: Reaction-Pathway Switching and Intermediate Transformations
Citations of This Product
Calculadoras de soluções
Revisões

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