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1143-46-0

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1143-46-0 Usage

Explanation

Different sources of media describe the Explanation of 1143-46-0 differently. You can refer to the following data:
1. The compound is composed of 16 carbon atoms, 24 hydrogen atoms, and 1 oxygen atom.
2. The compound contains a carbonyl group (C=O) bonded to two carbon-containing groups, which classifies it as a ketone.
3. The compound has a five-membered carbon ring, which is a cyclopentane ring.
4. A methyl group (CH3) is attached to the 3α-carbon of the cyclopentane ring.
5. An isopropylfuran-2-yl group (a furan ring with an isopropyl group attached to the 2nd carbon) is attached to the 2α-carbon of the cyclopentane ring.
6. The compound has an ethanone group (a two-carbon ketone, CH3CO-) attached to the cyclopentane ring.
7. The compound can be synthesized through various organic chemical reactions, which involve the formation of new chemical bonds and the transformation of simpler molecules into more complex ones.
8. The compound is used as a building block for creating new compounds with potential medicinal or industrial applications, such as drugs or chemical intermediates.
9. Due to its complex structure, the compound may have properties that make it useful as a fragrance or flavoring agent in the food and beverage industry.
10. The compound has a chiral center at the 1st carbon, with the (1S) configuration indicating the arrangement of the substituents in three-dimensional space.

Classification

Ketone

Cyclopentane Ring

Present

Methyl Substituent

3α-Position

Isopropylfuran-2-yl Substituent

2α-Position

Ethanone Group

Attached to the cyclopentane ring

Synthesis

Organic chemical reactions

Application

Pharmaceutical and chemical research

Potential Use

Fragrance or flavoring agent

Chirality

(1S) Configuration

Check Digit Verification of cas no

The CAS Registry Mumber 1143-46-0 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 1143-46:
(6*1)+(5*1)+(4*4)+(3*3)+(2*4)+(1*6)=50
50 % 10 = 0
So 1143-46-0 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-/m1/s1

1143-46-0SDS

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 furopelargone B

1.2 Other means of identification

Product number -
Other names (1S,2R,3R)-1r-Acetyl-2c-[3-isopropyl-2-furyl]-3c-methyl-cyclopentan

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:1143-46-0 SDS

1143-46-0Relevant articles and documents

A novel sesquiterpene peroxide from Alpinia japonica (THUNB.) MIQ.

Itokawa,Watanabe,Morita,et al.

, p. 2023 - 2027 (1985)

-

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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