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1,2,4-Oxadiazol-5-amine,3-(1,1-dimethylethyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114065-37-1 Structure
  • Basic information

    1. Product Name: 1,2,4-Oxadiazol-5-amine,3-(1,1-dimethylethyl)-(9CI)
    2. Synonyms: 1,2,4-Oxadiazol-5-amine,3-(1,1-dimethylethyl)-(9CI);3-(1,1-dimethylethyl)-1,2,4-Oxadiazol-5-amine;3-tert-butyl-1,2,4-oxadiazol-5-amine
    3. CAS NO:114065-37-1
    4. Molecular Formula: C6H11N3O
    5. Molecular Weight: 141.17104
    6. EINECS: N/A
    7. Product Categories: VARIOUSAMINE
    8. Mol File: 114065-37-1.mol
  • Chemical Properties

    1. Melting Point: 192 °C
    2. Boiling Point: 242.2±23.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.105±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 2.98±0.50(Predicted)
    10. CAS DataBase Reference: 1,2,4-Oxadiazol-5-amine,3-(1,1-dimethylethyl)-(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,2,4-Oxadiazol-5-amine,3-(1,1-dimethylethyl)-(9CI)(114065-37-1)
    12. EPA Substance Registry System: 1,2,4-Oxadiazol-5-amine,3-(1,1-dimethylethyl)-(9CI)(114065-37-1)
  • 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: 114065-37-1(Hazardous Substances Data)

114065-37-1 Usage

Chemical Class

Oxadiazoles Heterocyclic compounds containing an oxygen atom and two nitrogen atoms in a five-membered ring.

Specific Structure

1,2,4-Oxadiazol-5-amine,3-(1,1-dimethylethyl)-(9CI) Contains an amine group and a tert-butyl group.

Amine Group

-NH2

Tert-butyl Group

-C(CH3)3

Molecular Weight

142.16 g/mol

Pharmaceuticals

Used in the development of new drugs.

Agrochemicals

Utilized in the creation of new pesticides or herbicides.

Research Interest

Properties and potential applications are of interest to researchers and professionals in pharmaceuticals and agrochemicals industries.

Valuable Tool

Its molecular structure and properties make it a valuable tool for further research and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 114065-37-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,0,6 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 114065-37:
(8*1)+(7*1)+(6*4)+(5*0)+(4*6)+(3*5)+(2*3)+(1*7)=91
91 % 10 = 1
So 114065-37-1 is a valid CAS Registry Number.

114065-37-1SDS

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 3-tert-Butyl-[1,2,4]oxadiazol-5-ylamine

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:114065-37-1 SDS

114065-37-1Downstream Products

114065-37-1Relevant articles and documents

SYNTHESIS AND THERMOLYSIS OF SOME N-HYDROXIMOYL- AND N-HYDRAZONOYLAZOLES

Plenkiewicz, Jan,Zdrojewski, Tadeusz

, p. 675 - 710 (2007/10/02)

The reactions of nitrile oxides or nitrile imines with pyrazole, imidazole, 1,2,3- and 1,2,4-triazole or tetrazole derivatives yield the appropriate N-hydroximoyl- or N-hydrazonoylazoles.Thermolysis of 1-hydroximoyltetrazoles, depending on the nature of the substituents in the tetrazole ring, yields 1,2,4-oxadiazoles or 5-amino-1,2,4-oxadiazoles upon hydrazoic acid or nitrogen evolution.Under similar conditions, 1-hydrazonoyltetrazoles give 1,2,4-triazoles or 5-amino-1,2,4-triazoles while 2-hydrazonoyltetrazoles decompose to the dihydro-1,2,4,5-tetrazine derivatives.

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