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2(1H)-Pentalenone, 3-chloro-4,5,6,6a-tetrahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92007-30-2

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92007-30-2 Usage

Structure

Chlorinated derivative of pentalenone, a polycyclic aromatic hydrocarbon

Physical properties

+ Yellow solid
+ Soluble in organic solvents
+ Characteristic odor

Uses

Chemical research and synthesis

Unique properties

Presence of chlorine atom

Potential applications

Pharmaceuticals, materials science

Hazardous properties

Potentially hazardous, handle with caution

Check Digit Verification of cas no

The CAS Registry Mumber 92007-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,0,0 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92007-30:
(7*9)+(6*2)+(5*0)+(4*0)+(3*7)+(2*3)+(1*0)=102
102 % 10 = 2
So 92007-30-2 is a valid CAS Registry Number.

92007-30-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloro-4,5,6,6a-tetrahydro-1H-pentalen-2-one

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:92007-30-2 SDS

92007-30-2Downstream Products

92007-30-2Relevant academic research and scientific papers

ASYMMETRIC INDUCTION IN THE CYCLOADDITION REACTION OF DICHLOROKETENE WITH CHIRAL ENOL ETHERS. A VERSATILE APPROACH TO OPTICALLY ACTIVE CYCLOPENTENONE DERIVATIVES.

Greene, Andrew E.,Charbonnier, Florence

, p. 5525 - 5528 (2007/10/02)

Significant asymmetric induction has been observed in the cycloaddition reaction of dichloroketene with chiral enol ethers.The resultant diastereomeric cyclobutanones have been converted to synthetically useful α-chlorocyclopentenones in optically active form.

STRATEGY FOR CYCLOPENTENONE ANNULATION OF OLEFINS: A GENERAL PROTOCOL FOR BICYCLOENONE SYNTHESIS

Mehta, Goverdhan,Rao, K. Srinivas

, p. 1839 - 1842 (2007/10/02)

Several bicyclic α-chloro enones obtained through Greene annulation of cyclic olefins are shown to undergo efficient, two step, enone transposition via Luche reduction and aq. formic acid treatment.Application of this methodology to the formal synthesis of exaltone and (+/-)-muscone is described.

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