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Phenol, 2-(3,7-dimethyl-2,6-octadienyl)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73892-33-8

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73892-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73892-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,9 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73892-33:
(7*7)+(6*3)+(5*8)+(4*9)+(3*2)+(2*3)+(1*3)=158
158 % 10 = 8
So 73892-33-8 is a valid CAS Registry Number.

73892-33-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ortho-nerylphenol

1.2 Other means of identification

Product number -
Other names o-nerylphenol

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:73892-33-8 SDS

73892-33-8Downstream Products

73892-33-8Relevant academic research and scientific papers

Synthesis of stachybotrin C and all of its stereoisomers: Structure revision

Jacolot, Maiwenn,Jean, Mickael,Tumma, Naresh,Bondon, Arnaud,Chandrasekhar, Srivari,Van De Weghe, Pierre

, p. 7169 - 7175 (2013/08/23)

We disclose the first total synthesis of stachybotrin C, a potent neuroprotective natural compound. All of the four stereoisomers have been prepared and fully characterized with the aim to attribute the absolute configuration of the two adjacent stereocenters of the stachybotrin C.

Alkylation of phenol by nerol in the presence of organoaluminum compounds

Chukicheva,Fedorova,Koroleva,Kuchin

, p. 535 - 540 (2013/02/23)

Alkylation of aluminum phenolate by nerol and of phenol by nerol in the presence of the organoaluminum compounds aluminum phenolate and aluminum isopropylate was studied. The reaction products were isolated and characterized. Several features of the proce

Regio- and stereoselective copper-induced isomerization of 2-alkenyl 2-lithiophenyl ethers to 2-(2-alkenyl)phenols

Barluenga, Jose,Sanz, Roberto,Fananas, Francisco J.

, p. 6103 - 6106 (2007/10/03)

N-Allyl-N-(2-lithioallyl)aniline undergoes intramolecular carbometallation via 5-exo addition on treatment with CuCN. 2-Alkenyl 2-bromophenyl ethers rearrange to 2-(2-alkenyl)phenols by bromine-lithium exchange and further transmetallation with CuCN.

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