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74744-42-6

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74744-42-6 Usage

General Description

(Z)-4-Tridecen-6-yne is a chemical compound with the molecular formula C16H28. It is a type of alkyne, meaning it contains a carbon-carbon triple bond. (Z)-4-Tridecen-6-yne is typically used in organic synthesis and chemical research due to its ability to undergo various reactions, including addition reactions and oxidation reactions. It is commonly used as a building block for the synthesis of more complex organic compounds. (Z)-4-Tridecen-6-yne is a colorless liquid at room temperature and is flammable, requiring proper handling and storage. It is important to take appropriate safety precautions when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 74744-42-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,4 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74744-42:
(7*7)+(6*4)+(5*7)+(4*4)+(3*4)+(2*4)+(1*2)=146
146 % 10 = 6
So 74744-42-6 is a valid CAS Registry Number.

74744-42-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-Tridec-4-en-6-yne

1.2 Other means of identification

Product number -
Other names -

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:74744-42-6 SDS

74744-42-6Downstream Products

74744-42-6Relevant articles and documents

PHASE-TRANSFER VERSION OF THE WITTIG REACTION AND ITS STEREOCHEMISTRY IN THE ALIPHATIC SERIES

Khusid, A. Kh.,Kovalev, B. G.

, p. 62 - 67 (2007/10/02)

Alkyltriphenylphosphonium salts react with saturated α,β-ethylenic, α,β-acetylenic, and cyclic aliphatic aldehydes when heated with solid potassium carbonate to form the corresponding alkenes with preparative yields.The reaction is cis-stereoselective with saturated aldehydes and cis-stereospecific with unsaturated aldehydes.

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