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N-Allyl-1,7-dideazaadenine is an organic compound with the chemical formula C11H11N5. It is a brown solid and is known for its role in the preparation of pyrrolotriazines, which are a class of compounds with potential applications in various fields.

640735-22-4

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640735-22-4 Usage

Uses

1. Used in Pharmaceutical Industry:
N-Allyl-1,7-dideazaadenine is used as a key intermediate for the synthesis of pyrrolotriazines. These compounds have shown potential as therapeutic agents, particularly in the development of novel drugs for the treatment of various diseases.
2. Used in Chemical Research:
As a brown solid with unique chemical properties, N-Allyl-1,7-dideazaadenine can be utilized in chemical research to explore its reactivity, stability, and potential applications in the synthesis of other complex organic molecules.
3. Used in the Preparation of Pyrrolotriazines:
N-Allyl-1,7-dideazaadenine is used as a starting material or building block for the preparation of pyrrolotriazines. These compounds have demonstrated potential in various applications, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 640735-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,0,7,3 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 640735-22:
(8*6)+(7*4)+(6*0)+(5*7)+(4*3)+(3*5)+(2*2)+(1*2)=144
144 % 10 = 4
So 640735-22-4 is a valid CAS Registry Number.

640735-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-prop-2-enyl-1H-pyrrolo[2,3-b]pyridin-4-amine

1.2 Other means of identification

Product number -
Other names -

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:640735-22-4 SDS

640735-22-4Relevant academic research and scientific papers

Concise and Efficient Synthesis of 4-Fluoro-1H-pyrrolo[2,3-b]pyridine

Thibault, Carl,L'Heureux, Alexandre,Bhide, Rajeev S.,Ruel, Rejean

, p. 5023 - 5025 (2003)

(Equation presented) Two routes describing the preparation of 4-fluoro-1H-pyrrolo[2,3-b]pyridine (4a) from 1H-pyrrolo[2,3-b]pyridine N-oxide (1) are presented. Regioselective fluorination was achieved using either the Balz-Schiemann reaction or lithium-halogen exchange.

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