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N,N-dibenzyl-3-bromobutan-1-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1384850-07-0

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1384850-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1384850-07-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,8,5 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1384850-07:
(9*1)+(8*3)+(7*8)+(6*4)+(5*8)+(4*5)+(3*0)+(2*0)+(1*7)=180
180 % 10 = 0
So 1384850-07-0 is a valid CAS Registry Number.

1384850-07-0Downstream Products

1384850-07-0Relevant academic research and scientific papers

Dihydroxyphenyl Sulfonylisoindoline Derivatives

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Paragraph 058; 0104; 0121, (2018/06/12)

Provided are compounds that are inhibitors of pyruvate dehydrogenase kinase (PDK), and pharmaceutically acceptable salts, hydrides and stereoisomers thereof. The compounds are employed in pharmaceutical compositions, and methods of making and use, including treating a person in need thereof with an effective amount of the compound or composition.

Synthesis of 1-alkyl-2-(trifluoromethyl)azetidines and their regiospecific ring opening toward diverse α-(trifluoromethyl)amines via intermediate azetidinium salts

Kenis, Sara,D'Hooghe, Matthias,Verniest, Guido,Dang Thi, Tuyet Anh,Pham The, Chinh,Van Nguyen, Tuyen,De Kimpe, Norbert

, p. 5982 - 5992 (2012/09/21)

A convenient approach toward nonactivated 1-alkyl-2-(trifluoromethyl) azetidines as a new class of constrained azaheterocycles was developed starting from ethyl 4,4,4-trifluoroacetoacetate via imination, hydride reduction, chlorination, and base-induced ring closure. Furthermore, the reactivity profile of these 2-CF3-azetidines was assessed by means of quaternization and subsequent regiospecific ring opening at C4 of the azetidinium intermediates by oxygen, nitrogen, carbon, sulfur, and halogen nucleophiles, pointing to a clear difference in reactivity compared to azetidines bearing other types of electron-withdrawing groups at C2.

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