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5957-68-6

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5957-68-6 Usage

General Description

Camphenilol is a chemical compound that belongs to the class of terpenes, which are natural compounds found in plants. It is a colorless liquid with a characteristic pine-like odor and is commonly used in the fragrance and flavoring industry. Camphenilol is also known for its antifungal and antibacterial properties, making it useful in the development of products for medicinal and personal care applications. Additionally, it has been identified as a potential compound for use in the development of new pharmaceutical drugs due to its biological activities and low toxicity. Overall, camphenilol is a versatile compound with a range of potential industrial, medicinal, and pharmaceutical applications.

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 articles and documents

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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