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42027-37-2

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42027-37-2 Usage

Derivative of benzoic acid

It is a modified version of benzoic acid Benzoic acid is a simple aromatic carboxylic acid, and this compound has additional functional groups attached to its structure.

Contains an amino group

The presence of an amino group (-NH2) The amino group is responsible for the compound's potential biological activity and can form amide bonds with other molecules.

Potential applications in pharmaceuticals

It may be used in the development of new drugs The compound's unique structure and properties make it a promising candidate for further research in the pharmaceutical industry.

Potential applications in organic synthesis

It can be used as a building block for synthesizing other compounds The presence of various functional groups in the compound allows it to react with other molecules, making it a versatile starting material for organic synthesis.

Biological activity

2-[(E)-(2-chlorophenyl)methylidene]aminobenzoic acid may exhibit biological activity This means that it could interact with biological systems, such as enzymes or receptors, and potentially have therapeutic effects.

Potential candidate for further research and development

Its structure and properties make it a valuable subject for investigation The compound's unique features and potential applications make it an interesting target for further study in both the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 42027-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,0,2 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42027-37:
(7*4)+(6*2)+(5*0)+(4*2)+(3*7)+(2*3)+(1*7)=82
82 % 10 = 2
So 42027-37-2 is a valid CAS Registry Number.

42027-37-2Relevant articles and documents

Phl(OAc)2-mediated one-pot synthesis of benzoxazinones from anthranilic acids and aromatic aldehydes

Xie, Yuanyuan,Wang, Suping

experimental part, p. 123 - 126 (2012/09/22)

A novel way to synthesise 2-aryl-4H-benzo[d][1,3]oxazin-4-ones has been developed by the cyclisation of Schiff bases with (diacetoxyiodo)benzene. The salient features of this new protocol which starts from an anthranilic acid and an aromatic aldehyde, are

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