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1-cyclopentyl-1,4-diazepane(SALTDATA: 2tosilate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 245070-83-1 Structure
  • Basic information

    1. Product Name: 1-cyclopentyl-1,4-diazepane(SALTDATA: 2tosilate)
    2. Synonyms: 1-cyclopentyl-1,4-diazepane(SALTDATA: 2tosilate)
    3. CAS NO:245070-83-1
    4. Molecular Formula: C10H20N2
    5. Molecular Weight: 168.2792
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 245070-83-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 244.6°C at 760 mmHg
    3. Flash Point: 94.3°C
    4. Appearance: /
    5. Density: 0.969g/cm3
    6. Vapor Pressure: 0.0301mmHg at 25°C
    7. Refractive Index: 1.5
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 10.59±0.20(Predicted)
    11. CAS DataBase Reference: 1-cyclopentyl-1,4-diazepane(SALTDATA: 2tosilate)(CAS DataBase Reference)
    12. NIST Chemistry Reference: 1-cyclopentyl-1,4-diazepane(SALTDATA: 2tosilate)(245070-83-1)
    13. EPA Substance Registry System: 1-cyclopentyl-1,4-diazepane(SALTDATA: 2tosilate)(245070-83-1)
  • 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: 245070-83-1(Hazardous Substances Data)

245070-83-1 Usage

Class

Diazepane derivative

Structure

Unique structure with a cyclopentyl group attached to a 1,4-diazepane ring

Coordination chemistry

Potential use as a ligand

Organic synthesis

Building block for complex organic molecules

Pharmaceutical

Potential for development as a drug

Biological Activity

Investigated for antimicrobial and antifungal properties

Potential

Promising candidate for the development of new drugs

Further Study

Interesting compound for additional research and development in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 245070-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,0,7 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 245070-83:
(8*2)+(7*4)+(6*5)+(5*0)+(4*7)+(3*0)+(2*8)+(1*3)=121
121 % 10 = 1
So 245070-83-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H20N2/c1-2-5-10(4-1)12-8-3-6-11-7-9-12/h10-11H,1-9H2

245070-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Cyclopentyl-[1,4]diazepane

1.2 Other means of identification

Product number -
Other names 1-cyclopentyl-1,4-diazepane

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:245070-83-1 SDS

245070-83-1Upstream product

245070-83-1Relevant articles and documents

DIAZEPANES AS HISTAMINE H3 RECEPTOR ANTAGONISTS

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Page/Page column 45, (2009/09/05)

The invention relates to compounds of formula (I) wherein R1 to R8 and X1, X2 have the meaning as cited in the description and the claims. Said compounds are useful as Histamine H3 receptor antagonists. The invention also relates to pharmaceutical compositions, the preparation of such compounds as well as the production and use as medicament.

AZETIDINES AND CYCLOBUTANES AS HISTAMINE H3 RECEPTOR ANTAGONISTS

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Page/Page column 63-64, (2010/01/29)

The invention relates to compounds of formula (I) wherein R, R0, R1, m, n and X1 to X4 have the meaning as cited in the description and the claims. Said compounds are useful as Histamine H3 receptor antagonists. The invention also relates to pharmaceutical compositions, the preparation of such compounds as well as the production and use as medicament.

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