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2,5-Cyclohexadiene-1-carboxylic acid, 2-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25435-08-9

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25435-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25435-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,3 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25435-08:
(7*2)+(6*5)+(5*4)+(4*3)+(3*5)+(2*0)+(1*8)=99
99 % 10 = 9
So 25435-08-9 is a valid CAS Registry Number.

25435-08-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methoxycyclohexa-2,5-diene-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2,5-Cyclohexadiene-1-carboxylic acid,2-methoxy

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:25435-08-9 SDS

25435-08-9Upstream product

25435-08-9Relevant academic research and scientific papers

Non-Cryogenic, Ammonia-Free Reduction of Aryl Compounds

-

, (2022/03/31)

A method of reducing an aromatic ring or a cyclic, allylic ether in a compound includes preparing a reaction mixture including a compound including an aromatic moiety or a cyclic, allylic ether moiety, an alkali metal, and either ethylenediamine, diethylenetriamine, triethylenetetramine, or a combination thereof, in an ether solvent; and reacting the reaction mixture at from ?20° C. to 30° C. for a time sufficient to reduce a double bond in the aromatic moiety to a single bond or to reduce the cyclic, allylic ether moiety.

A HYBRID BIRCH-CLAISEN METHODOLOGY FOR ARYLATION AT ALLYLIC TERMINI: SYNTHESIS OF (+/-)-HERBERTENE

Chandrasekaran, S.,Turner, John V.

, p. 3799 - 3802 (2007/10/02)

A hybrid Birch-Claisen methodology has been developed for the regio- and stereo-controlled arylation of allyl groups, and applied to a synthesis of (+/-)-herbertene.

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