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180134-13-8

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180134-13-8 Usage

Physical state

Colorless liquid at room temperature The compound appears as a colorless liquid when it is not heated or cooled.

Versatility as a solvent

Ability to dissolve a wide range of organic substances This property makes it useful in various industries, as it can dissolve many different types of organic compounds.

Industrial applications

Pharmaceuticals, agrochemicals, and electronics The compound is used as a solvent in these industries due to its ability to dissolve a variety of organic substances.

Use in perfumes and fragrances

Production of perfumes and other fragrance products The compound is also utilized in the creation of scented products, likely due to its ability to dissolve fragrance components.

Hazardous properties

Ingestion or inhalation The compound can be harmful if it is swallowed or breathed in, which necessitates proper handling and storage.

Potential for irritation

Skin and eyes Contact with the compound may cause irritation to the skin and eyes, further emphasizing the importance of proper handling and storage.

Check Digit Verification of cas no

The CAS Registry Mumber 180134-13-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,1,3 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 180134-13:
(8*1)+(7*8)+(6*0)+(5*1)+(4*3)+(3*4)+(2*1)+(1*3)=98
98 % 10 = 8
So 180134-13-8 is a valid CAS Registry Number.

180134-13-8Downstream Products

180134-13-8Relevant articles and documents

2-Methoxy-4,6-bis(trifluoromethyl)phenyllithium: A new stable aryllithium useful as an intermediate to bis(trifluoromethyl)aromatics

Dmowski, Wojciech,Piasecka-Maciejewska, Krystyna

, p. 59 - 63 (2007/10/03)

A method for the preparation of 3,5-bis(trifluoromethyl)anisole (3) has been developed. Lithiation of 3 occurred exclusively at the position ortho to the CH3O group to give a thermally stable lithium derivative 6 which readily undergoes conventional reactions with a number of electrophiles. Formylation and carboxylation of 6 gave bis(trifluoromethyl) derivatives of salicylic aldehyde and salicylic acid 9-12 in good yields.

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