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  • 2881-62-1 Structure
  • Basic information

    1. Product Name: DI-SODIUM ACETYLIDE
    2. Synonyms: SODIUM ACETYLIDE;DI-SODIUM ACETYLIDE;Ethyne-1,2-diyldisodium
    3. CAS NO:2881-62-1
    4. Molecular Formula: C2Na2
    5. Molecular Weight: 70
    6. EINECS: 220-732-6
    7. Product Categories: N/A
    8. Mol File: 2881-62-1.mol
    9. Article Data: 1
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: °Cat760mmHg
    3. Flash Point: °C
    4. Appearance: /
    5. Density: g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: DI-SODIUM ACETYLIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: DI-SODIUM ACETYLIDE(2881-62-1)
    11. EPA Substance Registry System: DI-SODIUM ACETYLIDE(2881-62-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. RIDADR: 3132
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: 4.3
    8. PackingGroup: II
    9. Hazardous Substances Data: 2881-62-1(Hazardous Substances Data)

2881-62-1 Usage

Description

Di-sodium acetylide, a chemical compound with the formula Na2C2H, is composed of two sodium atoms bound to an acetylide ion. It is a highly reactive and unstable compound, known for its powerful basic properties. Due to its reactivity, it can release acetylene gas when it comes into contact with water or other protic solvents, which can lead to violent reactions and even explosions. The handling, storage, and use of di-sodium acetylide require strict safety protocols to mitigate the risks associated with its hazardous nature.

Uses

Used in Organic Synthesis:
Di-sodium acetylide is used as a reagent in organic synthesis for the preparation of various organic compounds. Its powerful basic nature allows it to deprotonate a wide range of substrates, facilitating the formation of new chemical bonds and enabling the synthesis of complex organic molecules.
Used in Chemical Production:
In the chemical industry, di-sodium acetylide is used as an intermediate in the production of other chemicals. Its reactivity makes it a valuable precursor for the synthesis of various chemical products, including pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Research and Development:
Due to its unique reactivity and properties, di-sodium acetylide is utilized in research and development for exploring new chemical reactions and developing innovative synthetic methods. Its ability to act as a strong base and participate in various types of chemical transformations makes it a valuable tool for chemists in academia and industry.
Used in Specialty Applications:
Although its use is limited due to its hazardous nature, di-sodium acetylide finds application in certain specialty areas where its unique properties are required. These applications may include the synthesis of specific compounds for advanced materials, catalysts, or other niche chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 2881-62-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,8 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2881-62:
(6*2)+(5*8)+(4*8)+(3*1)+(2*6)+(1*2)=101
101 % 10 = 1
So 2881-62-1 is a valid CAS Registry Number.
InChI:InChI=1/C2.2Na/c1-2;;/rC2Na2/c3-1-2-4

2881-62-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name DI-SODIUM ACETYLIDE

1.2 Other means of identification

Product number -
Other names disodium acetylide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2881-62-1 SDS

2881-62-1Relevant articles and documents

Metal Acetylide Elimination: The Key Step in the Cascade Decomposition and Transformation of Metalated Propargylamines

Flynn, Matthew T.,Blair, Victoria L.,Andrews, Philip C.

supporting information, p. 1225 - 1228 (2018/04/30)

Metal acetylide elimination facilitates a novel one-pot cascade metalation and elimination/addition route to a series of unsymmetrical secondary amines from the reaction of secondary propargylamines with organometallic reagents. Spectroscopic evidence suggests a dimetalated amido intermediate rather than an allene.

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