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6-(IsopropylaMino)pyridine-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 160017-00-5 Structure
  • Basic information

    1. Product Name: 6-(IsopropylaMino)pyridine-3-carbonitrile
    2. Synonyms: 6-(IsopropylaMino)pyridine-3-carbonitrile;6-(propan-2-ylamino)pyridine-3-carbonitrile
    3. CAS NO:160017-00-5
    4. Molecular Formula: C9H11N3
    5. Molecular Weight: 161.20374
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 160017-00-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-(IsopropylaMino)pyridine-3-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(IsopropylaMino)pyridine-3-carbonitrile(160017-00-5)
    11. EPA Substance Registry System: 6-(IsopropylaMino)pyridine-3-carbonitrile(160017-00-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 160017-00-5(Hazardous Substances Data)

160017-00-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160017-00-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,0,1 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 160017-00:
(8*1)+(7*6)+(6*0)+(5*0)+(4*1)+(3*7)+(2*0)+(1*0)=75
75 % 10 = 5
So 160017-00-5 is a valid CAS Registry Number.

160017-00-5SDS

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 6-(isopropylamino)nicotinonitrile

1.2 Other means of identification

Product number -
Other names 6-isopropylaminonicotinonitrile

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:160017-00-5 SDS

160017-00-5Relevant articles and documents

COMPOUNDS AND COMPOSITIONS FOR THE TREATMENT OF PARASITIC DISEASES

-

Page/Page column 107, (2014/06/11)

The present invention provides compounds of formula I: [INSERT FORMULA HERE] or a pharmaceutically acceptable salt, tautomer, or stereoisomer, thereof, wherein the variables are as defined herein. The present invention further provides pharmaceutical compositions comprising such compounds and methods of using such compounds for treating, preventing, inhibiting, ameliorating, or eradicating the pathology and/or symptomology of a disease caused by a Plasmodium parasite, such as malaria.

Modulators of S1P and Methods of Making And Using

-

Page/Page column 56-57, (2010/10/19)

The invention is directed to Compounds of Formula I: as well as methods of making and using the compounds.

3-Nitro-4-amino benzoic acids and 6-amino nicotinic acids are highly selective agonists of GPR109b

Skinner, Philip J.,Cherrier, Martin C.,Webb, Peter J.,Sage, Carleton R.,Dang, Huong T.,Pride, Cameron C.,Chen, Ruoping,Tamura, Susan Y.,Richman, Jeremy G.,Connolly, Daniel T.,Semple, Graeme

, p. 6619 - 6622 (2008/04/02)

A series of 3-nitro-4-substituted-aminobenzoic acids were prepared and found to act as potent and highly selective agonists of the orphan human GPCR GPR109b, a low affinity receptor for niacin. No activity was observed at the closely homologous high affinity niacin receptor, GPR109a. A second series, comprising 6-amino-substituted nicotinic acids was, also prepared and several analogues showed comparable activity to the nitroaryl series.

A Study of the Photochemically Induced Electron-Transfer Reactions Between Pyridinedicarbonitriles and Primary and Secondary Aliphatic Amines

Bernardi, Rosanna,Caronna, Tullio,Poggi, Gabriella,Vittimberga, Bruno M.

, p. 903 - 908 (2007/10/02)

A study on the photochemically induced electron-transfer from primary and secondary aliphatic amines as donors to pyridinecarbonitriles as the acceptor is reported.A comparison between the substitution positions and the spin density distributions, obtained via teoretical calculations using the 6-31+G basis set, shows some discrepancies, and forms the basis of a hypothesis on the mechanism of the reaction.

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