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CAS

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6333-30-8

2,6-bis[(dibenzylamino)methyl]cyclohexanone is a complex organic compound with the molecular formula C31H34N2O. It is characterized by a cyclohexanone ring, which is a six-membered carbon ring with a ketone group (C=O) at the 2 and 6 positions. Attached to these positions are dibenzylamino groups, which are derived from dibenzylamine, a compound consisting of two benzyl groups (C6H5CH2-) attached to an amino group (-NH2). The presence of these dibenzylamino groups contributes to the compound's steric bulk and potential reactivity. 2,6-bis[(dibenzylamino)methyl]cyclohexanone is of interest in organic chemistry, particularly in the synthesis of complex molecules and as a precursor in the preparation of various pharmaceuticals and other chemical products. Its structure and properties make it a valuable intermediate in the development of new compounds with specific therapeutic or industrial applications.

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  • 6333-30-8 Structure

  • Basic information

    1. Product Name: 2,6-bis[(dibenzylamino)methyl]cyclohexanone
    2. Synonyms:
    3. CAS NO:6333-30-8
    4. Molecular Formula: C36H40N2O*2ClH
    5. Molecular Weight: 516.7156
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6333-30-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 624°C at 760 mmHg
    3. Flash Point: 231.9°C
    4. Appearance: N/A
    5. Density: 1.103g/cm3
    6. Vapor Pressure: 1.72E-15mmHg at 25°C
    7. Refractive Index: 1.603
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,6-bis[(dibenzylamino)methyl]cyclohexanone(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,6-bis[(dibenzylamino)methyl]cyclohexanone(6333-30-8)
    12. EPA Substance Registry System: 2,6-bis[(dibenzylamino)methyl]cyclohexanone(6333-30-8)

  • 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: 6333-30-8(Hazardous Substances Data)

6333-30-8 Usage

Structure

A cyclohexanone ring with two dibenzylamino groups attached to the carbon atoms at the 2 and 6 positions

Type

Organic compound, derivative of cyclohexanone

Usage

Chemical intermediate in the synthesis of organic molecules and pharmaceuticals

+ Catalytic activity

Can catalyze various reactions in organic chemistry

+ Chiral auxiliary

Utility in asymmetric synthesis

+ Reagent in organic chemistry

Valued for its catalytic properties

Potential applications

Medicinal chemistry and drug development

Check Digit Verification of cas no

The CAS Registry Mumber 6333-30-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6333-30:
(6*6)+(5*3)+(4*3)+(3*3)+(2*3)+(1*0)=78
78 % 10 = 8
So 6333-30-8 is a valid CAS Registry Number.

6333-30-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclohexanone, 2,6-bis[[bis(phenylmethy)amino]methyl]-,dihydrochloride

1.2 Other means of identification

Product number -
Other names 2,6-bis-chloromethyl-pyrazine

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:6333-30-8 SDS

6333-30-8Downstream Products

6333-30-8Relevant articles and documents

Evaluation of some Mannich bases of cycloalkanones and related compounds for cytotoxic activity

Dimmock, JR,Sidhu, KK,Chen, M,Reid, RS,Allen, TM,et al.

, p. 313 - 322 (1993)

A number of Mannich bases of cycloalkanones and related quaternary ammonium compounds were prepared for cytotoxic evaluation in order to examine the theory that sequential release of alkylating agents produces increased bioactivity compared to related compounds containing only 1 potential alkylating site.Many of the compounds had significant activity against murine L1210 cells and various human tumours.Some correlations between structure and activity were noted but the biological data did not support the view that potential sequential liberation of cytotoxic species produced compounds with increased potency.The formation of various oximes and oxime benzoates as candidate prodrugs was achieved but in general these compounds were not cytotoxic at the concentrations utilized.This observation may be due to the fact that the oximes were much more stable in deuterated phosphate buffered saline over a period of 48 h at 37 deg than the Mannich bases, as revealed by 1H-NMR spectroscopy. Mannich bases / cytotoxic evaluations / prodrugs / 1H-NMR spectroscopy / structure-activity relationships

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