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2-METHYL-9-ACRIDINECARBALDEHYDE is an organic compound belonging to the acridine family, characterized by its tricyclic structure and aldehyde functional group. It exhibits unique chemical and fluorescent properties, making it a versatile molecule for various applications in research and pharmaceutical development.

70401-29-5

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70401-29-5 Usage

Uses

Used in Research Applications:
2-METHYL-9-ACRIDINECARBALDEHYDE is used as a reagent in the cleavage assay of rRNA by denaturing gel electrophoresis, a technique employed to study the structure and function of ribosomal RNA.
Used in Pharmaceutical Development:
2-METHYL-9-ACRIDINECARBALDEHYDE is used as a building block in the synthesis of peptide-acridine/acridone conjugates, which have potential applications as anticancer, antiviral, and antiprion drugs. These conjugates leverage the biological activity of acridine derivatives to target and combat various diseases and disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 70401-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,0 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70401-29:
(7*7)+(6*0)+(5*4)+(4*0)+(3*1)+(2*2)+(1*9)=85
85 % 10 = 5
So 70401-29-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H11NO/c1-10-6-7-15-12(8-10)13(9-17)11-4-2-3-5-14(11)16-15/h2-9H,1H3

70401-29-5 Well-known Company Product Price

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  • Aldrich

  • (220604)  2-Methyl-9-acridinecarboxaldehyde  97%

  • 70401-29-5

  • 220604-50MG

  • 5,180.76CNY

  • Detail

70401-29-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylacridine-9-carbaldehyde

1.2 Other means of identification

Product number -
Other names BIDD:GT0724

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:70401-29-5 SDS

70401-29-5Downstream Products

70401-29-5Relevant academic research and scientific papers

Reaction of diimines and benzyne

Aly, Ashraf A.,Mohamed, Nasr K.,Hassan, Alaa A.,Mourad, Aboul-Fetouh E.

, p. 1111 - 1118 (2007/10/03)

The reaction between benzyne and the Schiff bases 1a,b and 15a,b leads to the 1,4-bis(2-substituted acridin-10-yl)benzene 4a,b, the N- phenylarylamines 10a,b and the 10-(4-formylphenyl)-substituted acridines 11a,b (from 1a,b) and the 2-substituted acridine-10-carboxyaldehyde 18a,b (from 15a,b). Cyclohexyl (4-cyclohexyliminomethylbenzylidine)amine 1c reacts with benzyne by an ene-reaction to give cyclohexenyl[(4- cyclohexyliminomethylphenyl)benzylidine]amine 14.

Synthesis of 2-methylcarbamazepine, a new internal standard for chromatographic assays of carbamazepine (Tegretol)

Patton,Dudley

, p. 257 - 262,258,261 (2007/10/04)

The synthesis of 2-methyl-5H-dibenz[b,f]azepine-5-carboxamide (2-methylcarbamazepine, 2-MCBZ), a promising internal standard for chromatographic assays of the antiepileptic agent carbamazepine is described. N-(p-tolyl)anthranilic acid was utilized as a starting material for the synthesis of a key compound, 2,9-dimethylacridine, which was converted in two steps to 2-methyl-9-hydroxymethylacridan. The acridan, in the presence of polyphosphoric acid, was ring-expanded to form 2-methyl-5H-dibenz[b,f]azepine, this latter compound being converted by conventional reactions to its 5-carbamyl derivative, 2-MCBZ.

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