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(E)-5-decen-1-yne, with the molecular formula C10H16, is an alkyne chemical compound characterized by a triple bond between the carbon atoms at the 1 and 2 positions. It is a colorless liquid with a distinct odor and is insoluble in water. (E)-5-decen-1-yne is known for its reactivity and ability to participate in various chemical reactions, making it a versatile building block in the synthesis of different compounds.

53963-07-8

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53963-07-8 Usage

Uses

Used in Organic Synthesis:
(E)-5-decen-1-yne is used as a reagent in organic synthesis for its ability to undergo multiple chemical reactions, facilitating the creation of a wide range of compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (E)-5-decen-1-yne is utilized as a building block for the production of various pharmaceuticals, contributing to the development of new medications.
Used in Agrochemical Manufacturing:
(E)-5-decen-1-yne is also employed in the manufacture of agrochemicals, where its reactivity and ability to form different compounds are advantageous for creating effective products for agricultural use.
Used in Coatings, Adhesives, and Sealants Production:
Due to its reactive nature, (E)-5-decen-1-yne has applications in the production of coatings, adhesives, and sealants. Its ability to undergo various chemical reactions allows for the creation of products with specific properties tailored for different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 53963-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,6 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53963-07:
(7*5)+(6*3)+(5*9)+(4*6)+(3*3)+(2*0)+(1*7)=138
138 % 10 = 8
So 53963-07-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H16/c1-3-5-7-9-10-8-6-4-2/h1,9-10H,4-8H2,2H3/b10-9+

53963-07-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name dec-5-en-1-yne

1.2 Other means of identification

Product number -
Other names (E)-5-decen-1-yne

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:53963-07-8 SDS

53963-07-8Relevant academic research and scientific papers

PROCESS FOR PREPARING A 5-ALKEN-1-YNE COMPOUND, (6Z)-1,1-DIALKOXY-6-NONEN-2-YNE COMPOUND, (2E,6Z)-2,6-NONADIENAL AND (2E)-CIS-6,7-EPOXY-2-NONENAL, AND 1,1-DIALKOXY-6-NONEN-2-YNE COMPOUND

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, (2020/02/27)

The object of the present invention is to provide a process for preparing a 5-alken-1-yne compound efficiently at low costs and a process for preparing (2E,6Z)-2,6-nonadienal by making use of the aforesaid process for preparing the 5-alken-1-yne compound. There is provided a process for preparing a 5-alken-1-yne compound of the following formula (4): Y-Z-CR1═CR2—(CH2)2—C≡CH (4) in which Y in formula (4) represents a hydrogen atom or a hydroxyl group, the process comprising at least steps of: subjecting (i) an alkenylmagnesium halide compound prepared from a haloalkene compound of the following formula (1): Y-Z-CR1═CR2—(CH2)2-X1 (1) and (ii) an alkyne compound of the following formula (2): X2=C≡C—Si(R3)(R4)(R5) (2) to a coupling reaction to form a silane compound of the following formula (3): Y-Z-CR1═CR2—(CH2)2—C≡C—Si(R3)(R4)(R5) (3); and subjecting the silane compound (3) to a desilylation reaction to form the 5-alken-1-yne compound (4).

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