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Camphenilol is a terpene chemical compound derived from plants, characterized by its colorless liquid form and a distinctive pine-like odor. It is recognized for its antifungal and antibacterial properties, as well as its potential in pharmaceutical drug development due to its biological activities and low toxicity.

5957-68-6

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5957-68-6 Usage

Uses

Used in Fragrance and Flavoring Industry:
Camphenilol is utilized as a key ingredient in the fragrance and flavoring industry, capitalizing on its characteristic pine-like scent to enhance various products.
Used in Medicinal Applications:
In the medicinal field, Camphenilol is employed for its antifungal and antibacterial properties, making it a valuable component in the development of products for healthcare and personal care applications.
Used in Pharmaceutical Drug Development:
Camphenilol is recognized as a potential compound in the development of new pharmaceutical drugs, owing to its biological activities and low toxicity, which contribute to its potential as a therapeutic agent.

Check Digit Verification of cas no

The CAS Registry Mumber 5957-68-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,5 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5957-68:
(6*5)+(5*9)+(4*5)+(3*7)+(2*6)+(1*8)=136
136 % 10 = 6
So 5957-68-6 is a valid CAS Registry Number.

5957-68-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3-dimethyl-norbornan-2-ol

1.2 Other means of identification

Product number -
Other names Bicyclo[2.2.1]heptan-2-ol, 3,3-dimethyl-

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:5957-68-6 SDS

5957-68-6Relevant academic research and scientific papers

Deamination Reactions, 40. Decomposition of 3,3-, 5,5-, and 7,7-Dimethyl-2-norbornanediazonium Ions

Kirmse, Wolfgang,Brandt, Sigrid

, p. 2510 - 2523 (2007/10/02)

gem.-Dimethylnorbornyl cations (3, 5) were generated by decomposition of optically active diazonium ion precursors. 6,1- and 6,2-H shifts were detected by structural isomerization and racemization, respectively.Product distributions and optical activities were profoundly affected by the polarity of the solvent.In weakly polar solvents, substitution reactions were associated with much less racemization than hydrogen shifts.Our observations are incompatible with equilibrating open ions but are reasonably explained in terms of unsymmetrical ion pairs.

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