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26668-50-8

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26668-50-8 Usage

Chemical class

Acetamides

Trifluoromethyl group

Contains a CF3 group

Benzyl substituents

Two benzyl groups attached to the core structure

Hydroxylated substituents

One benzyl group with hydroxyl (-OH) group

Methoxylated substituents

One benzyl group with methoxy (-OCH3) group

Phenethylated substituents

The other benzyl group is connected to a phenyl ring through an ethyl (-CH2CH3) group

Synthetic chemical

It is a man-made compound with potential pharmacological properties

Potential applications

May have applications in drug development and research

Further research needed

Its specific biological and chemical properties, as well as potential uses, require additional scientific study and determination

Check Digit Verification of cas no

The CAS Registry Mumber 26668-50-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,6 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 26668-50:
(7*2)+(6*6)+(5*6)+(4*6)+(3*8)+(2*5)+(1*0)=138
138 % 10 = 8
So 26668-50-8 is a valid CAS Registry Number.

26668-50-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,2-trifluoro-N-[(3-hydroxy-4-methoxyphenyl)methyl]-N-[2-(4-hydroxyphenyl)ethyl]acetamide

1.2 Other means of identification

Product number -
Other names N-Trifluoracetyl-O-methylnorbelladin

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:26668-50-8 SDS

26668-50-8Relevant articles and documents

Enzymatic oxidative cyclisation reactions leading to dibenzoazocanes

Tozzi, Francesco,Ley, Steven V.,Kitching, Matthew O.,Baxendale, Ian R.

supporting information; experimental part, p. 1919 - 1922 (2010/10/02)

From simple N-isovanillyltyramine derivatives double oxidative biotransformations can be achieved using tyrosinase leading to the corresponding hydroxylated dibenzoazocanes. Georg Thieme Verlag Stuttgart.

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