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2881-62-1

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2881-62-1 Usage

General Description

Di-sodium acetylide is a chemical compound composed of two sodium atoms bound to an acetylide ion. It is a highly reactive and unstable compound that is often used in organic synthesis and in the production of other chemicals. Di-sodium acetylide is a powerful base and can react violently with water or other protic solvents, releasing acetylene gas and potentially causing explosions. Due to its hazardous nature, di-sodium acetylide must be handled with extreme caution and stored and used under strict safety protocols.

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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