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4-Chlor-2-(4-chlor-benzylamino)-benzoesaeure, also known as 4-chlor-2-(4-chlor-benzyl-amino)-benzoic acid, is a chemical compound with the molecular formula C14H11Cl2NO2. This organic compound features a benzoic acid structure with a chlorine atom at the 4-position and a benzylamine group at the 2-position, which is also substituted with a chlorine atom at the 4-position. It is a white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound is known for its potential applications in the development of drugs targeting the central nervous system and other therapeutic areas. Due to its chemical structure, it may exhibit properties such as reactivity with nucleophiles and electrophiles, which are important in organic synthesis.

4583-87-3

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4583-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4583-87-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,8 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4583-87:
(6*4)+(5*5)+(4*8)+(3*3)+(2*8)+(1*7)=113
113 % 10 = 3
So 4583-87-3 is a valid CAS Registry Number.

4583-87-3Downstream Products

4583-87-3Relevant academic research and scientific papers

Copper catalyzed C-N bond formation/C-H activation: Synthesis of aryl 4H-3,1-benzoxazin-4-ones

Munusamy, Sathishkumar,Venkatesan, Sathesh,Sathiyanarayanan, Kulathu Iyer

, p. 203 - 205 (2015)

We have developed a practical and efficient synthesis of 2-phenyl-4H-benzo[d][1,3]oxazine-4-one derivatives through copper catalyzed tandem reaction of 2-iodobenzoic acid with arylmethanamines under aerobic conditions. Compared to the literature methods toward the synthesis of 2-phenyl-4H-benzo[d][1,3]oxazine-4-one, the synthetic method reported in this Letter has broad substrate scope, mild reaction condition, and uses an inexpensive catalyst.

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