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Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-2,2-dimethyl(9CI) is a chemical compound characterized by a benzimidazole ring fused to a pyridine ring. It is a 1,2,3,4-tetrahydro derivative with two methyl groups attached to the carbon atoms in the tetrahydro ring. This unique molecular structure suggests potential biological activities and medicinal properties, making it a promising candidate for research and pharmaceutical applications.

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  • Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-2,2-dimethyl- (9CI)

    Cas No: 336106-30-0

  • USD $ 1.9-2.9 / Gram

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  • 336106-30-0 Structure
  • Basic information

    1. Product Name: Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-2,2-dimethyl- (9CI)
    2. Synonyms: Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-2,2-dimethyl- (9CI)
    3. CAS NO:336106-30-0
    4. Molecular Formula: C13H16N2
    5. Molecular Weight: 200.27954
    6. EINECS: N/A
    7. Product Categories: BENZIMIDAZOLE
    8. Mol File: 336106-30-0.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: Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-2,2-dimethyl- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-2,2-dimethyl- (9CI)(336106-30-0)
    11. EPA Substance Registry System: Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-2,2-dimethyl- (9CI)(336106-30-0)
  • 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: 336106-30-0(Hazardous Substances Data)

336106-30-0 Usage

Uses

Used in Pharmaceutical Research:
Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-2,2-dimethyl(9CI) is used as a research compound for exploring its potential interactions with various biological targets. Its structure and the presence of the tetrahydro group and methyl substituents may contribute to its pharmacokinetic properties, potentially enhancing its bioavailability and efficacy in drug development.
Used in Drug Development:
In the pharmaceutical industry, Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-2,2-dimethyl(9CI) is utilized as a lead compound for the discovery of new therapeutic agents. Its chemical structure and potential biological activities make it a valuable asset in the search for novel drugs with improved efficacy and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 336106-30-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,6,1,0 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 336106-30:
(8*3)+(7*3)+(6*6)+(5*1)+(4*0)+(3*6)+(2*3)+(1*0)=110
110 % 10 = 0
So 336106-30-0 is a valid CAS Registry Number.

336106-30-0SDS

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 2,2-dimethyl-3,4-dihydro-1H-pyrido[1,2-a]benzimidazole

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:336106-30-0 SDS

336106-30-0Downstream Products

336106-30-0Relevant articles and documents

Intermediacy of an N-heterocyclic carbene complex in the catalytic C-H activation of a substituted benzimidazole

Tan, Kian L.,Bergman, Robert G.,Ellman, Jonathan A.

, p. 3202 - 3203 (2007/10/03)

An N-heterocyclic carbene complex was found to be the active catalyst in the Rh(I)-catalyzed intramolecular coupling of an alkenyl group to a C-H bond of a substituted benzimidazole. Kinetic studies demonstrated that the catalytic cyclization is zero-orde

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