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1H,8H-3a,8a-methanoazulene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67313-66-0

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67313-66-0 Usage

Chemical structure

Tricyclic hydrocarbon compound with a methanoazulene core structure.

Physical state

Colorless liquid.

Color

Distinct blue color.

Odor

Pleasant, woody, and floral.

Industry applications

Commonly used in the fragrance and flavor industry.

Synthesis

Used as a building block in the synthesis of various organic compounds.

Starting material

Used as a starting material in the production of pharmaceuticals and fine chemicals.

Stability

Known for its high stability.

Resistance

Resistance to oxidation.

Versatility

Has versatile uses and properties.

Importance

An important component in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 67313-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,1 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67313-66:
(7*6)+(6*7)+(5*3)+(4*1)+(3*3)+(2*6)+(1*6)=130
130 % 10 = 0
So 67313-66-0 is a valid CAS Registry Number.

67313-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Tricyclo[5.3.1.0]undeca-2,4,9-triene

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:67313-66-0 SDS

67313-66-0Relevant academic research and scientific papers

New results in homoheptalene chemistry

Rueedi, Georg,Hansen, Hans-Juergen

, p. 1017 - 1047 (2007/10/03)

The thermal reaction of homoazulene (= bicyclo[5.3.1]undeca-1,3,5,7,9-pentaene; 2) with dimethyl acetylenedicarboxylate (ADM) in 1,2-dichloroethane (ClCH2CH2Cl) results, in contrast to an earlier report [5], in formation of not only

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