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Phenol, 2-(2-cyclohexen-1-yl)-6-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69914-70-1

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69914-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69914-70-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,1 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69914-70:
(7*6)+(6*9)+(5*9)+(4*1)+(3*4)+(2*7)+(1*0)=171
171 % 10 = 1
So 69914-70-1 is a valid CAS Registry Number.

69914-70-1SDS

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 2-cyclohex-2-en-1-yl-6-methoxyphenol

1.2 Other means of identification

Product number -
Other names 6-Methoxy-2-cycyclohexenyl-2-phenol

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:69914-70-1 SDS

69914-70-1Downstream Products

69914-70-1Relevant academic research and scientific papers

Microwave-assisted combined Mitsunobu reaction-Claisen rearrangement and microwave-assisted phenol oxidation: Rapid synthesis of 2,6-disubstituted-1,4- benzoquinone natural products

Jacob, Aouregan M.,Moody, Christopher J.

, p. 8823 - 8825 (2007/10/03)

Microwave irradiation of a phenol, an allylic alcohol, di-isopropyl azodicarboxylate and triphenylphosphine at 220-240°C for 30 min results in a combined Mitsunobu reaction and Claisen rearrangement to give the rearranged 2-allylphenol. Following the firs

A new approach to 2-(1-alkyl-cyclohex-2-en-1-yl) phenols

Essamkaoui,Mayrargue,Vierfond,Reynet,Moskowitz,Thal

, p. 2723 - 2728 (2007/10/02)

The synthesis of 2-(1-alkylcyclohex-2-en-1-yl) phenols has been accomplished in three steps: o-iodination of veratrole, palladium cross-coupling with cyclohexene and angular alkylation.

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