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(E)-3-Decen-1-yne is an organic compound with the molecular formula C10H16. It is a conjugated diene-yne, featuring a triple bond at the 1st carbon and a double bond at the 3rd carbon, with the double bond having the E (entgegen) configuration. This linear alkyne is characterized by its unique structure, which allows for various chemical reactions and applications in the synthesis of other organic compounds. It is an important intermediate in the production of certain fragrances, pharmaceuticals, and other specialty chemicals.

2807-10-5

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2807-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2807-10-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2807-10:
(6*2)+(5*8)+(4*0)+(3*7)+(2*1)+(1*0)=75
75 % 10 = 5
So 2807-10-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H16/c1-3-5-7-9-10-8-6-4-2/h1,5,7H,4,6,8-10H2,2H3/b7-5+

2807-10-5SDS

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 (E)-3-Decen-1-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

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More Details:2807-10-5 SDS

2807-10-5Relevant academic research and scientific papers

Construction of terminal conjugated enynes: Cu-mediated cross-coupling reaction of alkenyldialkylborane with (trimethylsilyl)ethynyl bromide

Hoshi, Masayuki,Kawamura, Noritsugu,Shirakawa, Kazuya

, p. 1961 - 1970 (2007/10/03)

The cross-coupling reaction of (E)- and (Z)-alk-1-enyldialkylborane with (trimethylsilyl)ethynyl bromide proceeds in the presence of a catalytic amount of copper(II) acetylacetonate and a base under extremely mild conditions to provide conjugated enynes w

Synthesis of allenic diols by samarium, diiodide-promoted coupling between alkynyloxiranes and ketones

Aurrecoechea, Jose M.,Alonso, Eva,Solay, Monica

, p. 3833 - 3850 (2007/10/03)

The SmI2-mediated reductive coupling between alkynyloxiranes and ketones provides a new route to 2,3-pentadiene-1,5-diols. The preferred stereochemistry observed in the coupling products is the result of the new C- C bond forming anti with respect to the opening epoxide ring. Yields and diastereoselectivities are dependent on the alkynyloxirane substitution pattern.

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