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Cyclopentene,1-propyl-, also known as 1-propylcyclopentene, is an organic compound with the molecular formula C8H14. It is a cyclic hydrocarbon with a five-membered ring structure, where one of the carbon atoms is attached to a propyl group (a three-carbon alkyl chain). Cyclopentene,1-propyl- is a colorless liquid with a pungent odor and is insoluble in water but soluble in organic solvents. It is used as an intermediate in the synthesis of various chemicals, including pharmaceuticals, agrochemicals, and fragrances. Cyclopentene,1-propyl- is also a precursor in the production of specialty polymers and can be used as a building block for more complex organic molecules.

3074-61-1

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3074-61-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3074-61-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,7 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3074-61:
(6*3)+(5*0)+(4*7)+(3*4)+(2*6)+(1*1)=71
71 % 10 = 1
So 3074-61-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H14/c1-2-5-8-6-3-4-7-8/h6H,2-5,7H2,1H3

3074-61-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Propyl-1-cyclopentene

1.2 Other means of identification

Product number -
Other names Cyclopentene,1-propyl

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:3074-61-1 SDS

3074-61-1Relevant academic research and scientific papers

Photolysis of azoalkane. Reactions and kinetics of the 1-cyclopropylcyclopentane-1,3-diyl biradical and the 1-cyclopropylcyclopentyl radical

Engel, Paul S.,Culotta, Anne Marie

, p. 2686 - 2696 (2007/10/02)

The cyclopropylcarbinyl (CPC) rearrangement rates of 1-cyclopropylcyclopentyl (10a) and 1-cyclopropylcyclohexyl (10b) radicals to yield 34a,b are found to be 1.45 × 107 and 1.1 × 107 s-1 at 24.7°C, respectively. These valu

Synthesis of Olefins from α-Chlorocarbonyl Compounds

Barluenga, Jose,Yus, Miguel,Concellon, Jose M.,Bernad, Pablo

, p. 677 - 692 (2007/10/02)

Olefins or diolefins with the double bonds in predetermined positions are obtained in moderate to good yields by treatment of α-chlorocarbonyl compounds with Grignard reagents and lithium in a single process.

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