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Tert-butyl oxazol-5-ylcarbamate is a chemical compound characterized by the molecular formula C9H15NO3. It is recognized for its stability and low toxicity, which makes it a valuable building block in the synthesis of various products. tert-butyl oxazol-5-ylcarbamate is particularly noted for its versatile reactivity and favorable properties, positioning it as a significant tool in the realm of chemical research and development.

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  • 1346809-07-1 Structure
  • Basic information

    1. Product Name: tert-butyl oxazol-5-ylcarbamate
    2. Synonyms: tert-butyl oxazol-5-ylcarbamate;5-Boc-aminooxazole
    3. CAS NO:1346809-07-1
    4. Molecular Formula: C8H12N2O3
    5. Molecular Weight: 184.19248
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1346809-07-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 225.3±13.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.192±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 12.45±0.70(Predicted)
    10. CAS DataBase Reference: tert-butyl oxazol-5-ylcarbamate(CAS DataBase Reference)
    11. NIST Chemistry Reference: tert-butyl oxazol-5-ylcarbamate(1346809-07-1)
    12. EPA Substance Registry System: tert-butyl oxazol-5-ylcarbamate(1346809-07-1)
  • 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: 1346809-07-1(Hazardous Substances Data)

1346809-07-1 Usage

Uses

Used in Organic Synthesis:
Tert-butyl oxazol-5-ylcarbamate is utilized as a reagent in organic synthesis, serving as a key component in the preparation of pharmaceuticals and agrochemicals. Its stability and low toxicity contribute to its widespread use in these applications.
Used in Drug Discovery and Development:
In the pharmaceutical industry, tert-butyl oxazol-5-ylcarbamate is employed as a building block for drug discovery and development. Its unique properties make it a promising candidate for the creation of new drugs with potential therapeutic benefits.
Used in the Development of Novel Materials and Catalysts:
Tert-butyl oxazol-5-ylcarbamate also finds application in the development of novel materials and catalysts. Its versatility in chemical reactions allows for the exploration of new material compositions and the enhancement of catalytic processes in various chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1346809-07-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,8,0 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1346809-07:
(9*1)+(8*3)+(7*4)+(6*6)+(5*8)+(4*0)+(3*9)+(2*0)+(1*7)=171
171 % 10 = 1
So 1346809-07-1 is a valid CAS Registry Number.
InChI:InChI=1S/C8H12N2O3/c1-8(2,3)13-7(11)10-6-4-9-5-12-6/h4-5H,1-3H3,(H,10,11)

1346809-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl oxazol-5-ylcarbamate

1.2 Other means of identification

Product number -
Other names tert-butyl N-(1,3-oxazol-5-yl)carbamate

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:1346809-07-1 SDS

1346809-07-1Relevant articles and documents

Formation of 6-Azaindoles by Intramolecular Diels-Alder Reaction of Oxazoles and Total Synthesis of Marinoquinoline A

Jhaveri, Dishit P.,Osano, Mana,Wipf, Peter

, p. 2215 - 2219 (2020)

A new variant of the intramolecular Diels-Alder oxazole (IMDAO) cycloaddition that provides direct access to 6-azaindoles was developed. The IMDAO reaction was applied in a total synthesis of the aminophenylpyrrole-derived alkaloid marinoquinoline A, also

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