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Cyclopentanone, 2-(1-cyclopenten-1-yl)-, also known as 2-cyclopenten-1-yl-cyclopentan-1-one, is an organic compound with the molecular formula C9H12O. It is a cyclic ketone with a cyclopentenyl group attached to the 2-position of the cyclopentanone ring. Cyclopentanone,2-(1-cyclopenten-1-yl)- is characterized by its unique structure, which features a five-membered cyclopentanone ring and a five-membered cyclopentenyl ring. It is an important intermediate in the synthesis of various organic compounds and can be used in the preparation of pharmaceuticals, fragrances, and other specialty chemicals. The compound is typically synthesized through various chemical reactions, such as the condensation of cyclopentanone with cyclopentene, and can be further functionalized to yield a wide range of derivatives.

7027-34-1

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7027-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7027-34-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,2 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7027-34:
(6*7)+(5*0)+(4*2)+(3*7)+(2*3)+(1*4)=81
81 % 10 = 1
So 7027-34-1 is a valid CAS Registry Number.

7027-34-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclopentanol,2-cyclopentylidene

1.2 Other means of identification

Product number -
Other names cyclopentylidene-cyclopentanol

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:7027-34-1 SDS

7027-34-1Upstream product

7027-34-1Relevant academic research and scientific papers

RuCl3 catalyses aldol condensations of aldehydes and ketones

Iranpoor, Nasser,Kazemi, Foad

, p. 9475 - 9480 (1998)

Anhydrous RuCl3 catalyses the efficient cross aldol condensations of different ketones with various aromatic aldehydes in sealed tube under solvent free conditions without the occurrence of any self condensations. Regioselective self condensation reaction of some ketones and aldehydes are also described. The catalytic effect of Ru(III) is shown by performing similar reactions under thermal conditions without catalyst.

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