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4-Heptyn-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32398-68-8

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32398-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32398-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,9 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 32398-68:
(7*3)+(6*2)+(5*3)+(4*9)+(3*8)+(2*6)+(1*8)=128
128 % 10 = 8
So 32398-68-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O/c1-3-5-6-7(8)4-2/h3-4H2,1-2H3

32398-68-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name hept-4-yn-3-one

1.2 Other means of identification

Product number -
Other names 4-heptyn-3-one

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:32398-68-8 SDS

32398-68-8Relevant academic research and scientific papers

An improved synthesis of dialkylcyclopropenones

Netland, Kjetil Andreas,Gundersen, Lise-Lotte,Rise, Frode

, p. 1767 - 1777 (2007/10/03)

Dialkylcyclopropenones are formed in high yields when alkynes are treated with chloroform-butyllithium in THF at - 78 °C followed by acidic hydrolysis of the dichlorocyclopropene intermediates at low temperatures.

Chromium(II) Reagents; 1. Reduction of α-Acetylenic Ketones to trans-Enones

Smith, Amos B.,Levenberg, Patricia A.,Suits, Joan Z.

, p. 184 - 189 (2007/10/02)

The preparation and chromium(II)-induced reduction of twelve α-acetylenic ketones are reported.In general only trans-olefinic products were observed; the yields ranged from 40-84percent.A particular advantage of this protocol is its selectivity, thereby permitting use with a wide variety of functionalities.

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