80258-99-7 Usage
Chemical class
Acridine carboxylic acids
Explanation
1-CHLORO-9,10-DIHYDRO-9-OXO-4-ACRIDINECARBOXYLIC ACID belongs to the class of acridine carboxylic acids, which are organic compounds derived from acridine.
2. Derivative of acridine
Explanation
This chemical compound is a derivative of acridine, meaning it is structurally related to acridine and has similar properties.
3. Chlorine atom at the 1-position
Explanation
The compound contains a chlorine atom attached to the 1-position of the acridine ring, which influences its chemical properties and reactivity.
4. Carboxylic acid group at the 4-position
Explanation
A carboxylic acid group (-COOH) is present at the 4-position of the acridine ring, contributing to the compound's acidity and potential for forming salts or esters.
5. Potential biological activities
Explanation
1-CHLORO-9,10-DIHYDRO-9-OXO-4-ACRIDINECARBOXYLIC ACID has been studied for its possible biological activities, such as antimicrobial and antitumor properties.
6. Applications in pharmaceuticals
Explanation
Due to its potential biological activities, this compound may be used in the development of pharmaceuticals for treating various diseases and conditions.
7. Applications in agrochemicals
Explanation
The compound may also have uses in the agrochemical industry, potentially serving as a pesticide, herbicide, or fungicide.
8. Versatile chemical
Explanation
1-CHLORO-9,10-DIHYDRO-9-OXO-4-ACRIDINECARBOXYLIC ACID is a versatile chemical with potential applications in various fields, including medicine, agriculture, and research.
Check Digit Verification of cas no
The CAS Registry Mumber 80258-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,5 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 80258-99:
(7*8)+(6*0)+(5*2)+(4*5)+(3*8)+(2*9)+(1*9)=137
137 % 10 = 7
So 80258-99-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H8ClNO3/c15-9-6-5-8(14(18)19)12-11(9)13(17)7-3-1-2-4-10(7)16-12/h1-6H,(H,16,17)(H,18,19)
80258-99-7Relevant articles and documents
A nitrogen hetero-cycloalkyl amino quinacridineone-4-amide compound and its preparation method and application
-
, (2017/01/31)
The invention provides an azo-heteroaromatic cycloalkylaminoacridone-4-amide compound which is shown in a formula I or a formula II as shown in the specification, as well as a preparation method and application thereof. In the formula I and the formula II
Potential Antitumor Agents. 46. Structure-Activity Relationships for Acridine Monosubstituted Derivatives of the Antitumor Agent N--9-aminoacridine-4-carboxamide
Rewcastle, Gordon W.,Atwell, Graham J.,Chambers, David,Baguley, Bruce C.,Denny, William A.
, p. 472 - 477 (2007/10/02)
A series of monosubstituted derivatives of the new antitumor agent N--9-aminoacridine-4-carboxamide has been prepared, bearing methyl, methoxy, and chloro groups at available acridine positions.The physicochemical properties and an
Synthesis of Substituted 9-Oxo-9,10-dihydroacridine-4-carboxylic Acids. I. Factors Affecting the Direction of Ring Closure of Substituted N-(2-Carboxyphenylamino)benzoic Acids
Stewart, Georgina M.,Rewcastle, Gordon W.,Denny, William A.
, p. 1939 - 1950 (2007/10/02)
The cyclodehydration of 16 substituted N-(2-carboxyphenylamino)benzoic acids to substituted 9-oxo-9,10-dihydroacridine-4-carboxylic acids with conc.H2SO4, POCl3 and ethyl polyphosphate (epp) has been studied by h.p.l.c.Direction of ring closure can be qua
