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Bicyclo[3.3.1]nonan-2-ol, also known as borneol or isoborneol, is a bicyclic monoterpene alcohol with the molecular formula C10H18O. It is a colorless, crystalline solid that is widely used in the fragrance and flavor industries due to its camphor-like odor and minty taste. This organic compound is found in various essential oils, such as those from rosemary, thyme, and eucalyptus, and is known for its insect-repellent properties. Bicyclo[3.3.1]nonan-2-ol is also used in the synthesis of various pharmaceuticals and as a stabilizer in the production of certain chemicals.

2568-14-1

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2568-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2568-14-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2568-14:
(6*2)+(5*5)+(4*6)+(3*8)+(2*1)+(1*4)=91
91 % 10 = 1
So 2568-14-1 is a valid CAS Registry Number.

2568-14-1SDS

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 bicyclo[3.3.1]nonan-4-ol

1.2 Other means of identification

Product number -
Other names 2-Bicyclo<Bicyclo[3.3.1]nonan-2-ol,endo

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:2568-14-1 SDS

2568-14-1Relevant academic research and scientific papers

Fragmentierungsreaktionen an Carbonylverbindungen mit β-staendigen elektronegativen Substituenten, XXXIII 3-Oxatricyclo1,4>undec-4-en, ein stark gespannter Vierring-Enolether

Gerdes, Hero,Javeri, Shailaja,Marschall, Helga

, p. 1907 - 1920 (2007/10/02)

The behaviour of β-keto tosylates against nucleophiles has been investigated.The keto tosylate 6 underwent intramolecular cyclization with KOtBu in ether to produce exclusively the four-membered O-alkylated product 18 (the title compound).The substitution products 5 or 7 are obtained from 6 with NaOMe in methanol or KCN in DMSO, resp.Reaction of 6 with MeLi yielded the diol 13.The keto tosylate 31 reacted with MeLi analogously to form the diol 28, whereas with MeMgI a mixture of the Grob fragmentation product 33 and the alcohol 32 (via 28 by H2O elimination) was produced.Similarly keto tosylate 22b and MeMgI yielded the alcohol 27. - The non-enolizable keto tosylate 44 undergoes very slow reaction wih NaOH/MeOH to produce 41, 42, and 45 in low yield.

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