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4-Amino-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile is a chemical compound with the molecular formula C7H5N5. It is a heterocyclic compound, specifically a pyrrolo[2,3-d]pyrimidine derivative, which features a pyrrole ring fused to a pyrimidine ring. The compound has an amino group at the 4-position and a nitrile group at the 5-position. It is a white to off-white solid and is soluble in polar solvents such as water and methanol. 4-Amino-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile is of interest in medicinal chemistry, particularly in the development of potential therapeutic agents, due to its unique structure and the presence of functional groups that can be further modified or used in the formation of more complex molecules.

1500-90-9

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1500-90-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1500-90-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,0 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1500-90:
(6*1)+(5*5)+(4*0)+(3*0)+(2*9)+(1*0)=49
49 % 10 = 9
So 1500-90-9 is a valid CAS Registry Number.

1500-90-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-7H-pyrrolo[2,3-d]pyrimidine-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-amino-5-cyanopyrrolo<2,3-d>pyrimidine

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:1500-90-9 SDS

1500-90-9Downstream Products

1500-90-9Relevant academic research and scientific papers

Nitrile reductase from Geobacillus kaustophilus: A potential catalyst for a new nitrile biotransformation reaction

Wilding, Birgit,Winkler, Margit,Petschacher, Barbara,Kratzer, Regina,Glieder, Anton,Klempier, Norbert

, p. 2191 - 2198 (2012/11/06)

The cloning, expression and characterization of a nitrile reductase (NRed) from the thermophile Geobacillus kaustophilus is reported. The enzyme shows a 12-fold increase in activity in response to a temperature change from 25 °C to 65 °C. The substrate scope regarding its biocatalytic applicability was investigated by testing a range of common nitriles. The narrow substrate range observed for the wild-type enzyme prompted the rational design of GkNRed active site mutants based on a previously published homology model from Bacillus subtilis. The activities of the mutants and the wild-type enzyme were investigated in their structure-function relationship regarding the natural substrate 7-cyano-7-deazaguanine (preQ0) as well as a range of synthesized preQ0-like substrate structures. A distinct dependence of the wild-type enzyme activity on specific structural modifications of the natural substrate was observed. Two non-natural nitriles derived from preQ 0 could be reduced to their corresponding amino compounds. Copyright

Synthesis, Cytotoxicity, and Antiviral Activity of Some Acyclic Analogues of the Pyrrolopyrimidine Nucleoside Antibiotics Tubercidin, Toyocamycin, and Sangivamycin

Gupta, Pranab K.,Daunert, Sylvia,Nassiri, M. Reza,Wotring, Linda L.,Drach, John C.,Townsend, Leroy B.

, p. 402 - 408 (2007/10/02)

A number of 7-pyrrolopyrimidine derivatives that are structurally related to toyocamycin and sangivamycin and the seco nucleosides of tubercidin, toyocamycin and sangivamycin were prepared and tested for their biolo

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