Formate（FA） - UltraPureChrom™, for ULC-MS, 0.1% in Acetonitrile , CAS No.64-18-6

CAS: 64-18-6 Cat. No.: F298778 分子式: CH₂O₂ 分子量: 46.03 Beilstein Registry Number: 1209246 EC番号: 200-579-1

グレード＆純度 UltraPureChrom™, for ULC-MS, 0.1% in Acetonitrile

Synonyms

FORMIC ACID [EP MONOGRAPH] | Acidum formicum | CCG-266004 | Formic acid, purum, >=85% | FORMICUM ACIDUM [HPUS] | Kyselina mravenci [Czech] | STL264243 | FORMIC ACID [INCI] | Formic acid, ACS reagent, >=96.0% | FORMIC ACID [HSDB] | Formic acid, AR, >=98% |

Storage

Room temperature,Argon charged

Shipped In

FedEx DG Service

概要

Formic acid can be used as a reagent for: carbonyl compounds and nitro compounds

Co Nx catalyzed one pot reductive amination reaction to synthesize secondary amines.

Photoreduction of polycyclic and heterocyclic nitroaromatic hydrocarbons to form corresponding amines.

Pd catalyzed chemical selective hydrogenation of olefins to form saturated hydrocarbons.

仕様

同義語

FORMIC ACID [EP MONOGRAPH] | Acidum formicum | CCG-266004 | Formic acid, purum, >=85% | FORMICUM ACIDUM [HPUS] | Kyselina mravenci [Czech] | STL264243 | FORMIC ACID [INCI] | Formic acid, ACS reagent, >=96.0% | FORMIC ACID [HSDB] | Formic acid, AR, >=98% |

仕様と純度

UltraPureChrom™, for ULC-MS, 0.1% in Acetonitrile

保管条件

Room temperature,Argon charged

入荷

FedEx DG Service

等級

for ULC-MS, UltraPureChrom™

名前と識別子

カノニカル・スマイル

C(=O)O

IUPAC Name

formic acid

InChIKey

BDAGIHXWWSANSR-UHFFFAOYSA-N

INCHI

1S/CH2O2/c2-1-3/h1H,(H,2,3)

異性体SMILES

C(=O)O

WGKドイツ

1

UN番号

1779

包装グループ

II

分子量

46.03

Beilstein

1209246

Reaxy-Rn

1209246

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1209246&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • 分類 Carboxylic acids and derivatives
      • Subclass Carboxylic acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• 分類: Carboxylic acids and derivatives
• Subclass: Carboxylic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acids
• Alternative Parents: Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• 説明: This compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
• External Descriptors: Straight chain fatty acids - Saturated fatty acids

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

関連ターゲット（非人間）

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作用メカニズム

化学的性質と物理的性質

• 感度: Hygroscopic
• 屈折率: 1.3690 - 1.3730
• 引火点（°F）: 121.1 °F
• 引火点（°C）: 49.5 °C
• 沸点（°C）: 100-101°C
• 融点（°C）: 8.2-8.4°C
• 分子量: 46.025 g/mol
• XLogP3: -0.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 46.0055 Da
• Monoisotopic Mass: 46.0055 Da
• Topological Polar Surface Area: 37.300 Ų
• Heavy Atom Count: 3
• Formal Charge: 0
• Complexity: 10.300
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1