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4141-38-2

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4141-38-2 Usage

General Description

2,4-diphenyl-1,3-dioxolane is a chemical compound with the molecular formula C14H12O2. It is a colorless liquid with a sweet odor and is primarily used as a solvent in various industrial applications. 2,4-diphenyl-1,3-dioxolane is also used in the manufacture of perfumes, pharmaceuticals, and other organic compounds. It has low solubility in water and is considered to have low toxicity. However, prolonged exposure to this compound may lead to irritation of the skin, eyes, and respiratory system. It is important to handle this chemical with care and use appropriate safety measures when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 4141-38-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,4 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4141-38:
(6*4)+(5*1)+(4*4)+(3*1)+(2*3)+(1*8)=62
62 % 10 = 2
So 4141-38-2 is a valid CAS Registry Number.

4141-38-2Relevant articles and documents

Iron oxide-pillared clay catalyzed the synthesis of acetonides from epoxides

Trikittiwong, Piyarat,Sukpirom, Nipaka,Shimazu, Shogo,Chavasiri, Warinthorn

, p. 104 - 107 (2015/03/18)

FeOx-pillared clays (FeOx-pillared bentonite, FeOx-pillared hectorite and FeOx-pillared taeniolite) were synthesized by the intercalation of FeCl3 into clay interlayers and calcination. The synthesize

Phosphonium salts and aldehydes from the convenient, anhydrous reaction of aryl acetals and triphenylphosphine hydrobromide

Ramanathan, Mani,Hou, Duen-Ren

, p. 98 - 108 (2013/05/09)

The reactions of aryl acetals/ketals and triphenylphosphine hydrobromide gave the corresponding aldehydes/ketones and alkyl phosphonium bromides. This reaction was applied to convert acetals/ketals to the corresponding aldehydes/ketones under an anhydrous

Stereoelectronic effects in the DIBAL reduction of aryl-1,2-ethanediol benzylidene acetals

Gauthier Jr., Donald R,Szumigala Jr., Ronald H,Armstrong III, Joseph D,Volante

, p. 7011 - 7014 (2007/10/03)

Reduction of benzylidene acetal 8 with DIBAL-H selectively gave 4 in 89% yield. 1-Aryl-1,2-diol benzylidene acetals display unusual regioselectivity with electron withdrawing groups on the aryl group.

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