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1-(bicyclo[3.3.1]non-6-en-3-yl)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66483-55-4

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66483-55-4 Usage

Structure

Bicyclic

Classification

Ketone derivative

Subtype

Alpha, beta-unsaturated ketone

Presence of functional groups

Carbon-carbon double bond adjacent to the carbonyl group

Applications

a. Organic synthesis
b. Preparation of pharmaceuticals and agrochemicals
c. Production of flavor and fragrance compounds

Reactivity

Imparts specific reactivity due to its bicyclic structure

Stability

Exhibits stability properties

Utility

Useful building block in the chemical industry

Check Digit Verification of cas no

The CAS Registry Mumber 66483-55-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,8 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66483-55:
(7*6)+(6*6)+(5*4)+(4*8)+(3*3)+(2*5)+(1*5)=154
154 % 10 = 4
So 66483-55-4 is a valid CAS Registry Number.

66483-55-4SDS

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-(3-bicyclo[3.3.1]non-6-enyl)ethanone

1.2 Other means of identification

Product number -
Other names 3-endo-Acetylbicyclo<3.3.1>non-6-ene

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:66483-55-4 SDS

66483-55-4Downstream Products

66483-55-4Relevant academic research and scientific papers

Experimental and Computed Chiroptical Properties of Thioketones

Lightner, David A.,Bouman, Thomas D.,Wijekoon, W. M.,Hansen, Aage E.

, p. 934 - 944 (2007/10/02)

(+)-(1S,3R)-4S(a)-Methyladamantane-2-thione (1), (+)-(1S,3R)-4R(e)-methyladamantane-2-thione (3), and (+)-(1S,3R)-4,4-dideuterioadamantane-2-thione (5) were prepared and their circular dichroism (CD) spectra measured and compared with those of the corresponding ketones.The long-wavelength n-?* CD transitions of the thiones and parent ketones agree in sign and magnitude.Ab initio calculations on thioacetone and methyl ethyl thioketone in the random-phase approximation (RPA) in several basis sets lead to assignment of the two lowest energy observed bands as n-?* and ?-?* and a third band composed of closely spaced and n-4s and ?-?* excitations.Similar calculations on 1 and 3 and their keto analogues yield n-?* rotatory strengths (R) in excellent agreement with experimental and support the applicability of the ketone octant rule to thioketones.An origin-independent analysis of the computed R values suggests that the same mechanism for n-?* optical activity operates in both classes of compounds.

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