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10313-06-1

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10313-06-1 Usage

Type of compound

Alkyne

Structure

Contains a triple bond between two carbon atoms

Reactivity

Highly reactive

Volatility

Highly volatile

Usage

Commonly used in organic synthesis and chemical research

Building block

Useful in the synthesis of various other organic compounds

Safety

Should be handled with caution and proper safety measures should be taken when working with it in a laboratory setting

Role

Plays an important role in the development of new chemical products and processes

Check Digit Verification of cas no

The CAS Registry Mumber 10313-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,1 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10313-06:
(7*1)+(6*0)+(5*3)+(4*1)+(3*3)+(2*0)+(1*6)=41
41 % 10 = 1
So 10313-06-1 is a valid CAS Registry Number.

10313-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name hepta-1,3-diyne

1.2 Other means of identification

Product number -
Other names 1,3-HEPTADIYNE

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:10313-06-1 SDS

10313-06-1Relevant articles and documents

Synthesis of enynones from alkynes, alkynyl ketones and aromatic aldehydes using the TiCl4/Et3N reagent system

Periasamy, Mariappan,Karunakar, Galla V.,Bharathi, Pandi

, p. 566 - 568 (2007/10/03)

Alkynyltitanium species, prepared in situ from alk-1-ynes using the TiCl4/Et3N reagent system, react with aromatic aldehydes to give enynones 2 in 49-38% yields. Reaction of alkynyl aryl ketones with aromatic aldehydes and the TiCls

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