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Benzenecarboximidothioic acid, N-phenyl-, phenyl ester, also known as N-phenylbenzimidoyl chloride or N-phenylbenzimidoyl phenyl ester, is an organic compound with the chemical formula C13H10N2S. It is a derivative of benzenecarboximidothioic acid, where a phenyl group is attached to the nitrogen atom, and a phenyl ester group is present. Benzenecarboximidothioic acid, N-phenyl-, phenyl ester is a white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is known for its reactivity and can undergo various chemical reactions, such as nucleophilic substitution and addition reactions, making it a valuable building block in organic synthesis.

4494-63-7

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4494-63-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4494-63-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,9 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4494-63:
(6*4)+(5*4)+(4*9)+(3*4)+(2*6)+(1*3)=107
107 % 10 = 7
So 4494-63-7 is a valid CAS Registry Number.

4494-63-7Relevant academic research and scientific papers

Pd-Catalyzed regioselective iminothiolation of alkynes: A remarkable effect of the CF3 group of iminosulfides

Minami, Yasunori,Kuniyasu, Hitoshi,Sanagawa, Atsushi,Kambe, Nobuaki

supporting information; experimental part, p. 3744 - 3747 (2010/11/04)

Pd-catalyzed iminothiolation of alkynes took place to afford 4-SR substituted 1-azadienes regioselectively.

THE BEHAVIOUR OF α-DIKETONE MONO-, AND DI-IMINE SYSTEMS TOWARDS 2,4-BIS(PHENYLTHIO)-1,3-DITHIA-2,4-DIPHOSPHETANE-2,4-DISULFIDE (JAPANESE REAGENT, JR)

Hafez, Taghrid S.

, p. 87 - 94 (2007/10/02)

2,4-Bis(phenylthio)-1,3-dithia-2,4-diphosphetane-2,4-disulfide (Japanese reagent, JR, 4) reacts with benzil monoanils 1a-c, in boiling THF to give the respective 1,2-diphenyl-2-(phenylthio)-2--ethane-1-thiones 6a-c.Compound 6a was also prepared by the action of (P2S5)x on 1a followed by addition of thiophenol to the produced thione 5a.Benzil dianils 2a-c reacted with reagent 4 in dry toluene to yield the respective phenyl-(phenylthio)--methane 8a-c.Possible reaction mechanisms were considered and structures of the new products were supported by compatible analytical and spectroscopic evidences. Key words: Benzil mono-imine; di-imines; Japanese reagent; homolytic fission, radical mechanism..

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