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21020-26-8

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21020-26-8 Usage

Class of compound

Alkyne

Physical state

Clear, colorless liquid at room temperature

Flammability

Highly flammable

Common uses

Reagent in organic synthesis, building block for other chemical compounds

Applications

Production of pharmaceuticals, agrochemicals, and fine chemicals

Solvent use

Industrial processes

Handling precautions

Handle with caution due to flammability and potential health hazards

Check Digit Verification of cas no

The CAS Registry Mumber 21020-26-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,2 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21020-26:
(7*2)+(6*1)+(5*0)+(4*2)+(3*0)+(2*2)+(1*6)=38
38 % 10 = 8
So 21020-26-8 is a valid CAS Registry Number.

21020-26-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethylpent-1-yne

1.2 Other means of identification

Product number -
Other names 1-Pentyne,3-ethyl

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:21020-26-8 SDS

21020-26-8Relevant articles and documents

REACTIONS OF 3-ALKYL- AND 3,3-DIALKYL-1-BROMOALLENES WITH ORGANOCUPRATES: EFFECTS OF THE NATURE OF THE CUPRATE REAGENT ON THE REGIO- AND STEREOSELECTIVITY

Caporusso, Anna Maria,Polizzi, Carmela,Lardicci, Luciano

, p. 6073 - 6076 (2007/10/02)

Organocuprates induce 1,3- and direct substitution in 3-alkyl- and 3,3-dialkyl-1-bromo-1,2-dienes leading respectively to either terminal acetylenes or allenic hydrocarbons.The nature of the cuprate exerts a prominent role in determining both the regio- and the stereochemistry of these reactions.

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