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1-[(1R)-3α-Methyl-2α-(3-isopropylfuran-2-yl)cyclopentan-1β-yl]ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1143-45-9

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1143-45-9 Usage

Type of compound

Cyclopentanone derivative

Uses

a. Synthesis of pharmaceutical and organic compounds
b. Flavoring agent

Color

Colorless liquid

Odor

Fruity

Solubility

Soluble in organic solvents (e.g., ethanol, diethyl ether)

Biological properties

a. Potential anti-inflammatory properties
b. Potential anti-microbial properties

Ecological significance

Volatile chemical present in certain plant species

Application in pest control

Used as a pheromone component for insect control

Check Digit Verification of cas no

The CAS Registry Mumber 1143-45-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,4 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1143-45:
(6*1)+(5*1)+(4*4)+(3*3)+(2*4)+(1*5)=49
49 % 10 = 9
So 1143-45-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H22O2/c1-9(2)12-7-8-17-15(12)14-10(3)5-6-13(14)11(4)16/h7-10,13-14H,5-6H2,1-4H3/t10-,13-,14-/m0/s1

1143-45-9SDS

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 1-[(1R,2S,3S)-3-methyl-2-(3-propan-2-ylfuran-2-yl)cyclopentyl]ethanone

1.2 Other means of identification

Product number -
Other names furopelargone A

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:1143-45-9 SDS

1143-45-9Relevant academic research and scientific papers

TWO NEW SESQUITERPENOIDS (ALPINOLIDE AND HANAMOYL) FROM ALPINIA JAPONICA (THUNB.) MIQ.

Itokawa, Hideji,Morita, Hiroshi,Watanable, Kinzo,Takase, Akiko,Iitaka, Yoichi

, p. 1687 - 1690 (1984)

Two new sesquiterpenoids (alpinolide and hanamyol) were isolated from Alpinia japonica (THUNB.) MIQ. and the structures were determined by the spectral, the chemical evidence and X-ray analysis.The chemical transformation of hanalpinol into alpinolide may suggest the biogenesis of furopelargone A and B.

Novel Guaiane- and Secoguaiane- Type Sesquiterpenes from Alpinia japonica (THUNB.) MIQ.

Itokawa, Hideji,Morita, Hiroshi,Osawa, Kenji,Watanabe, Kinzo,Iitaka, Yoichi

, p. 2849 - 2859 (2007/10/02)

Three novel guaiane-type sesquiterpenes, hanalpinone (I), isohanalpinone (II), and alpinenone (III), and two novel secoguaiane-type sesquiterpenes, alpinolide peroxide (IV) and 6-hydroxyalpinolide (V) have been isolated from the rhizomes of Alpinia japonica.Their structures were determined by spectroscopic methods, chemical conversions, and X-ray analysis.Their biosynthetic relationships with previously identified sesquiterpenes from Alpinia japonica are discussed.Keywords-Alpinia japonica; Zingiberaceae; sesquiterpene; guaiane; secoguaiane; peroxide; X-ray analysis; 13C-NMR; biosynthesis

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