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1H-Pyrrolo[2,3-d]pyrimidin-4-amine, 5,6-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82703-33-1

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82703-33-1 Usage

Structure

Pyrrolopyrimidine core with an amine group and two methyl substituents at the 5 and 6 positions

Type of compound

Heterocyclic organic compound

Use in pharmaceutical research

Study of kinase inhibitors and potential anticancer agents

Value in synthesis

Valuable intermediate for the synthesis of biologically active molecules

Therapeutic potential

Ability to interact with specific cellular targets and modulate biological pathways, but further research is needed to understand its pharmacological properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 82703-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,0 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82703-33:
(7*8)+(6*2)+(5*7)+(4*0)+(3*3)+(2*3)+(1*3)=121
121 % 10 = 1
So 82703-33-1 is a valid CAS Registry Number.

82703-33-1Relevant academic research and scientific papers

Method for organically synthesizing 5,6-dimethyl-7H-pyrrolo[2,3]pyrimidin-4-amine

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Paragraph 0030-0032, (2018/11/22)

The invention discloses a method for organically synthesizing 5,6-dimethyl-7H-pyrrolo[2,3]pyrimidin-4-amine. The method comprises the following steps: using 3-hydroxyl-2-butanone and alpha-methyl benzylamine as raw materials, performing reflux stirring in

Synthesis of 7-Unsubstituted 7H-Pyrrolopyrimidines

Pichler, Herbert,Folkers, Gerd,Roth, Hermann J.,Eger, Kurt

, p. 1485 - 1505 (2007/10/02)

The title compounds 4 are obtained by N-7 dealkylation of the 2-furanylmethyl, 2-thiophenylmethyl, or 1-phenylethyl group from 2a-g and 10 a-j with polyphosphoric acid.In contrast to the 2-furanylmethyl group the 2-thiophenylmethyl and 1-phenylethyl group

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