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400074-59-1

1,2,4-Triazolo[4,3-a]pyridine-3-acetonitrile,5,6,7,8-tetrahydro-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 400074-59-1 Structure

  • Basic information

    1. Product Name: 1,2,4-Triazolo[4,3-a]pyridine-3-acetonitrile,5,6,7,8-tetrahydro-(9CI)
    2. Synonyms: 1,2,4-Triazolo[4,3-a]pyridine-3-acetonitrile,5,6,7,8-tetrahydro-(9CI)
    3. CAS NO:400074-59-1
    4. Molecular Formula: C8H10N4
    5. Molecular Weight: 162.1918
    6. EINECS: N/A
    7. Product Categories: AMINETERTIARY
    8. Mol File: 400074-59-1.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: 1,2,4-Triazolo[4,3-a]pyridine-3-acetonitrile,5,6,7,8-tetrahydro-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2,4-Triazolo[4,3-a]pyridine-3-acetonitrile,5,6,7,8-tetrahydro-(9CI)(400074-59-1)
    11. EPA Substance Registry System: 1,2,4-Triazolo[4,3-a]pyridine-3-acetonitrile,5,6,7,8-tetrahydro-(9CI)(400074-59-1)

  • 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: 400074-59-1(Hazardous Substances Data)

400074-59-1 Usage

Explanation

This is the full name of the compound, which is a heterocyclic chemical compound.

Explanation

The molecular formula represents the number of carbon (C), hydrogen (H), and nitrogen (N) atoms in the compound.

Explanation

The compound has a ring structure containing different types of atoms, specifically carbon and nitrogen.

Explanation

The compound features a ring with five atoms, including three nitrogen atoms and two carbon atoms.

Explanation

It is commonly used as a building block for the synthesis of various biologically active compounds.

Explanation

The compound can exhibit different pharmacological activities, making it a valuable target for drug discovery and development.

Explanation

It is important to handle this compound with care due to its potential hazards and toxicity.

Explanation

Proper safety measures should be taken when working with this compound to minimize the risk of exposure and potential harm.

Type of Compound

Heterocyclic

Ring Structure

Five-membered ring

Application

Pharmaceutical industry

Pharmacological Activities

Anti-bacterial, anti-inflammatory, and anti-cancer properties

Potential Hazards

Toxicity

Safety Precautions

Handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 400074-59-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,0,0,7 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 400074-59:
(8*4)+(7*0)+(6*0)+(5*0)+(4*7)+(3*4)+(2*5)+(1*9)=91
91 % 10 = 1
So 400074-59-1 is a valid CAS Registry Number.

400074-59-1SDS

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 5,6,7,8-Tetrahydro[1,2,4]triazolo[4,3-a]pyridin-3-ylacetonitrile

1.2 Other means of identification

Product number -
Other names 3'-CH2CN-ddT

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:400074-59-1 SDS

400074-59-1Downstream Products

400074-59-1Relevant articles and documents

Study of reactions of lactim ethers with cyanoacetohydrazide

Nilov,Granik

, p. 1636 - 1641 (2007/10/03)

Main pathways in reactions of lactim ethers with cyanoacetic acid hydrazide depend on the ring size of the starting lactim ether. Five-membered O-methylbutyrolactim produces pre-dominantly 3-amino-4-(pyrrolidin-2-ylidene)-4, 5-dihydropyrazol-5-one, whereas condensation of six-and seven-membered lactim ethers (O-methylvalero-and O-methylcaprolactim, respectively) affords the corresponding polymethylenetriazoles as the major products.

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