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68291-93-0

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68291-93-0 Usage

General Description

The chemical compound (2H-1,3-benzodioxol-5-ylmethyl)(propyl)amine, also known as safrole, is an organic compound with a benzodioxole backbone and an attached propylamine group. It is commonly used in the production of fragrances and flavors due to its pleasant odor. Safrole is also a precursor in the synthesis of the recreational drug MDMA (ecstasy) and has been used historically as a flavoring agent in root beers and sassafras tea. However, due to its potential carcinogenic and toxic effects, safrole is regulated and its use in food and consumer products is restricted in many countries.

Check Digit Verification of cas no

The CAS Registry Mumber 68291-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,9 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68291-93:
(7*6)+(6*8)+(5*2)+(4*9)+(3*1)+(2*9)+(1*3)=160
160 % 10 = 0
So 68291-93-0 is a valid CAS Registry Number.

68291-93-0Downstream Products

68291-93-0Relevant articles and documents

ORGANIC COMPOUNDS

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Paragraph 0040; 0041, (2016/10/31)

This disclosure relates to taste modifiers of formula (I) wherein, n is 1, 2 or 3; R1 is selected from C1-C5 alkyl, C1-C5 hydroxyalkyl, C1-C5 dihydroxyalkyl and —CHYCOOH wherein

Preparation of benzolactams by Pd(OAC)2-catalyzed direct aromatic carbonylation

Orito, Kazuhiko,Horibata, Akiyoshi,Nakamura, Takatoshi,Ushito, Harumi,Nagasaki, Hideo,Yuguchi, Motoki,Yamashita, Satoshi,Tokuda, Masao

, p. 14342 - 14343 (2007/10/03)

We developed a new method for Pd(II)-catalyzed direct aromatic carbonylation in a phosphine-free catalytic system using Pd(OAc)2 and Cu(OAc)2 in an atmosphere of CO gas containing air. The carbonylation proceeded with ortho-palladation, inducing a remarkable site selectivity to afford a variety of five- or six-membered benzolactams from secondary ω-arylalkylamines, such as N-alkylbenzylamines or N-alkylphenethylamines. Copyright

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