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Butanamide, N-(1,1-dimethylethyl)-3-oxo-2-(phenylmethylene)-, also known as 2-benzylidene-N,N-dimethyl-3-oxobutanamide, is a chemical compound with the molecular formula C13H15NO2. It is a derivative of butanamide, featuring a 3-oxo group (a carbonyl group adjacent to a carbonyl or carboxyl group) and a phenylmethylene group (a phenyl group attached to a methylene group). Butanamide, N-(1,1-dimethylethyl)-3-oxo-2-(phenylmethylene)- is characterized by its amide structure, with a nitrogen atom bonded to a carbonyl group and an alkyl group. It is an organic compound that can be used in various chemical reactions and synthesis processes, particularly in the pharmaceutical and chemical industries.

3532-55-6

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3532-55-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3532-55-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,3 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3532-55:
(6*3)+(5*5)+(4*3)+(3*2)+(2*5)+(1*5)=76
76 % 10 = 6
So 3532-55-6 is a valid CAS Registry Number.

3532-55-6Relevant academic research and scientific papers

1,3-Oxazines and Related Compounds. XIII. Reaction of Acyl Meldrum's Acids with Schiff Bases Giving 2,3-Disubstituted 5-Acyl-3,4,5,6-tetrahydro-2H-1,3-oxazine-4,6-diones and 2,3,6-Trisubstituted 2,3-Dihydro-1,3-oxazin-4-ones

Yamamoto, Yutaka,Watanabe, Yukiyoshi,,Ohnishi, Shuhei

, p. 1860 - 1870 (2007/10/02)

The reaction of Schiff bases (2) with various acyl Meldrum's acids (1) were investigated.Refluxing of 1 and 2 in benzene caused an exchange reaction of the acetone moiety of 1 with the Schiff base moiety through the intermediate acylketenes 11 formed in s

Reaction of 2,2,6-trimethyl-1,3-dioxin-4-one with Imines

Masayuki, Sato,Ogasawara, Hiromichi,Yoshizumi, Eriko,Kato, Tetsuzo

, p. 1902 - 1909 (2007/10/02)

The reaction of 2,2,6-trimethyl-1,3-dioxin-4-one (diketene-acetone adduct) (1) with imines was investigated.Heating of the adduct 1 with N-(1-phenylethylidene)aniline (6a) gave 6-methyl-1,2-diphenyl-4(1H)-pyridone 7a.Similar treatment of N-benzylideneanil

REACTION OF 2,2,6-TRIMETHYL-1,3-DIOXIN-4-ONE WITH SCHIFF BASE

Sato, Masayuki,Ogasawara, Hiromichi,Yoshizumi, Eriko,Kato, Tetsuzo

, p. 297 - 300 (2007/10/02)

Heating of 2,2,6-trimethyl-1,3-dioxin-4-one (1) with Schiff bases (2a-f) gave 2,3-disubstituted 6-methyl-1,3-oxazin-4-ones (4a-f).N-Benzylidene-tert-butylamine, under the similar condition, gave acetoacetamide derivative (3g) and acetylazetidinone derivative (5).

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