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N,N'-(phenyl-ethanediyl)-bis-benzamide, also known as 1,2-phenylenebis(N-benzoylacetamide), is an organic compound with the molecular formula C20H17NO3. It is a white crystalline solid that is soluble in organic solvents such as ethanol and acetone. N,N'-(phenyl-ethanediyl)-bis-benzamide is characterized by its amide and benzene ring structures, with a phenyl-ethanediyl linker connecting two benzamide groups. It is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Due to its specific chemical structure, it may exhibit properties such as reactivity with nucleophiles and electrophiles, which can be exploited in chemical reactions. The compound's physical and chemical properties, such as its melting point, boiling point, and solubility, are important considerations in its handling and use in chemical processes.

95006-06-7

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95006-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95006-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,0 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 95006-06:
(7*9)+(6*5)+(5*0)+(4*0)+(3*6)+(2*0)+(1*6)=117
117 % 10 = 7
So 95006-06-7 is a valid CAS Registry Number.

95006-06-7Downstream Products

95006-06-7Relevant academic research and scientific papers

Iodine(III)-promoted intermolecular diamination of alkenes

Souto, Jose A.,Gonzalez, Yolanda,Iglesias, Alvaro,Zian, Debora,Lishchynskyi, Anton,Muniz, Kilian

supporting information; experimental part, p. 1103 - 1111 (2012/07/17)

A rapid and productive vicinal diamination of alkenes takes place in the presence of a hypervalent iodine(III) reagent and bissulfonimides as nitrogen sources. A total of more than 60 examples are presented. The reaction is characterized by its robustness and its wide substrate scope: it proceeds selectively with both terminal and internal alkenes and tolerates a range of functional groups.

An Expedient Synthesis of Vicinal Diamines from Alkenes and Cycloalkenes

Osowska-Pacewicka, Krystyna,Zwierzak, Andrzej

, p. 505 - 508 (2007/10/02)

A new procedure for the facile preparation of various vicinal diamines is developed that utilizes diethyl N-(β-bromoalkyl)phosphoramidates 2 easily accessible by ionic addition of diethyl N,N-dibromophosphoramidate (DBPA) to alkenes and cycloalkenes 1.Cru

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