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Benzoic acid-(2-bromoacetyl-anilide) is a chemical compound with the molecular formula C15H12BrNO2. It is a derivative of benzoic acid, where the carboxyl group (-COOH) is replaced by a 2-bromoacetyl-anilide group. benzoic acid-(2-bromoacetyl-anilide) is characterized by the presence of a bromine atom attached to the acetyl group, which is further connected to an aniline moiety. The structure of benzoic acid-(2-bromoacetyl-anilide) provides it with unique chemical properties, making it useful in various applications, such as in the synthesis of pharmaceuticals and other organic compounds. Its specific reactivity and functional groups can be exploited in chemical reactions, potentially leading to the formation of new compounds with different properties and applications.

4688-61-3

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4688-61-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4688-61-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,8 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4688-61:
(6*4)+(5*6)+(4*8)+(3*8)+(2*6)+(1*1)=123
123 % 10 = 3
So 4688-61-3 is a valid CAS Registry Number.

4688-61-3Relevant academic research and scientific papers

Treatment of Olefinic Amides with NBS in Water: Synthesis of Monobromo- A nd Multibromobenzoxazines

Cao, Wen-Bin,Ji, Shun-Jun,Xu, Xiao-Ping,Zhang, Xu

, p. 3805 - 3814 (2019)

Treatment of olefinic amides with N-bromosuccinimide (NBS) in water is reported. Monobromobenzoxazines were mainly formed at room temperature, while at 80? °C multibromobenzoxazines were preferentially generated. Mechanism studies showed that the reaction might proceed via a cascade of electrophilic addition at the C=C bond followed by electrophilic substitution at the aromatic ring. No additives are required in this protocol.

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