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111265-51-1

1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,N-methyl-,[1S-(1alpha,5alpha,6alpha)]-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,N-methyl-,[1S-(1alpha,5alpha,6alpha)]-

    Cas No: 111265-51-1

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  • 111265-51-1 Structure

  • Basic information

    1. Product Name: 1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,N-methyl-,[1S-(1alpha,5alpha,6alpha)]-(9CI)
    2. Synonyms: 1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,N-methyl-,[1S-(1alpha,5alpha,6alpha)]-(9CI)
    3. CAS NO:111265-51-1
    4. Molecular Formula: C6H11N3O
    5. Molecular Weight: 141.17
    6. EINECS: N/A
    7. Product Categories: AMIDE
    8. Mol File: 111265-51-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.28±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 18.90±0.20(Predicted)
    10. CAS DataBase Reference: 1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,N-methyl-,[1S-(1alpha,5alpha,6alpha)]-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,N-methyl-,[1S-(1alpha,5alpha,6alpha)]-(9CI)(111265-51-1)
    12. EPA Substance Registry System: 1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,N-methyl-,[1S-(1alpha,5alpha,6alpha)]-(9CI)(111265-51-1)

  • 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: 111265-51-1(Hazardous Substances Data)

111265-51-1 Usage

Molecular structure

Bicyclic, containing a diazabicyclo ring and a carboxamide group

Stereochemistry

1S, 1α, 5α, and 6α configurations

Functional groups

Diazabicyclo ring, carboxamide, and N-methyl groups

Role

Used as a catalyst in various chemical reactions

Applications

a. Formation of urethanes
b. Synthesis of organic compounds
c. Potential use in pharmaceuticals and materials science

Advantages

a. Facilitates reactions under mild conditions
b. Versatility in catalyzing a variety of reactions

Importance

Valuable compound in the field of organic chemistry due to its efficiency and versatility in catalyzing chemical reactions

Check Digit Verification of cas no

The CAS Registry Mumber 111265-51-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,2,6 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 111265-51:
(8*1)+(7*1)+(6*1)+(5*2)+(4*6)+(3*5)+(2*5)+(1*1)=81
81 % 10 = 1
So 111265-51-1 is a valid CAS Registry Number.

111265-51-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-Diazabicyclo[3.1.0]hexane-5-carboxamide,N-methyl-,[1S-(1alpha,5alpha,6alpha)]-(9CI)

1.2 Other means of identification

Product number -
Other names Azanator

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:111265-51-1 SDS

111265-51-1Relevant articles and documents

1,2-Acyl Migration to an Electron-deficient Nitrogen Atom: a New Rearrangement of Diaziridines without Ring Opening

Denisenko, Sergei N.,Shustov, Gennady V.,Kostyanovsky, Remir G.

, p. 1275 - 1276 (2007/10/02)

5-Acyl-1,6-diazabicyclohexane (1) on treatment with t-butyl hypochlorite affords the corresponding N-chloro-derivative (2) which rearranges easily into 6-acyl-5-chloro-1,6-diazabicyclohexane (3) with a 1,2-shift of the acyl group.

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