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4-pyridin-4-yl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine is a complex organic compound with the molecular formula C14H16N4. It is a derivative of imidazo[4,5-c]pyridine, which is a heterocyclic compound with a pyridine ring fused to an imidazole ring. This specific compound features a pyridine group at the 4-position, and the imidazo[4,5-c]pyridine core is fully saturated, indicating the presence of four additional hydrogen atoms in the molecule. It is likely to be a synthetic compound with potential applications in medicinal chemistry or as a building block for more complex molecules. The compound's structure and properties would be of interest to researchers in the field of organic synthesis and drug development.

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  • 7271-08-1 Structure
  • Basic information

    1. Product Name: 4-pyridin-4-yl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine
    2. Synonyms: 4-pyridin-4-yl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine;4-{3H,4H,5H,6H,7H-imidazo[4,5-c]pyridin-4-yl}pyridine
    3. CAS NO:7271-08-1
    4. Molecular Formula: C11H12N4
    5. Molecular Weight: 200.23978
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 7271-08-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 461.6±40.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.241±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 13.91±0.40(Predicted)
    10. CAS DataBase Reference: 4-pyridin-4-yl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-pyridin-4-yl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine(7271-08-1)
    12. EPA Substance Registry System: 4-pyridin-4-yl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine(7271-08-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 7271-08-1(Hazardous Substances Data)

7271-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7271-08-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,7 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7271-08:
(6*7)+(5*2)+(4*7)+(3*1)+(2*0)+(1*8)=91
91 % 10 = 1
So 7271-08-1 is a valid CAS Registry Number.

7271-08-1SDS

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 4-pyridin-4-yl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine

1.2 Other means of identification

Product number -
Other names 4-(4-Pyridyl)-4,5,6,7-tetrahydro-imidazo<4,5-c>pyridin

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:7271-08-1 SDS

7271-08-1Relevant articles and documents

4,5,6,7-Tetrahydroimidazo-[4,5-c]-pyridine derivatives

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, (2008/06/13)

New 4,5,6,7-tetrahydroimidazo-[4,5-c]-pyridine derivatives are disclosed, and more particularly derivatives of Formula I STR1 where R1 is hydrogen or an alkyl having from 1 to 4 carbon atoms; R2 is hydrogen, an alkyl having from 1 to 4 carbon atoms, a cycloalkyl having from 3 to 6 carbon atoms, phenyl or a heterocycle; R3 is hydrogen, a saturated or unsaturated straight or branched alkyl having from 1 to 6 carbon atoms, a cycloalkyl having from 3 to 6 carbon atoms, benzoyl or phenyl; and X is O, S or NR4 where R4 is hydrogen, an alkyl having from 1 to 4 carbon atoms, cyano, amino, nitro or acylamino; Or pharmaceutically acceptable acid addition salts thereof. Also disclosed is a process of preparing these compounds which comprises condensing an appropriate 4,5,6,7-tetrahydroimidazo-[4,5-c]-pyridine with an appropriate alkyl isocyanate, alkyl isothiocyanate or substituted S-methyl thiourea, preferably in a solvent such as ethanol, acetonitrile or dioxane, usually under reflux for from 4 to 12 hours. The products can be isolated by crystallization as free bases or as salts of pharmaceutically acceptable acids. The new compounds have proved to be well tolerated and to inhibit both the number of experimental ulcers and the gastric secretion in experimental animals. Thus, they should prove useful in the therapy of gastric and duodenal ulcers in man.

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