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2-PROPYL[1,3]OXAZOLO[4,5-B]PYRIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104711-71-9

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104711-71-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104711-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,1 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104711-71:
(8*1)+(7*0)+(6*4)+(5*7)+(4*1)+(3*1)+(2*7)+(1*1)=89
89 % 10 = 9
So 104711-71-9 is a valid CAS Registry Number.

104711-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Propyl[1,3]oxazolo[4,5-b]pyridine

1.2 Other means of identification

Product number -
Other names Octanal,2-propyl

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:104711-71-9 SDS

104711-71-9Downstream Products

104711-71-9Relevant academic research and scientific papers

Synthesis of novel heterocycles: Oxazolo[4,5-b]pyridines and oxazolo[4,5-d]pyrimidines

Doise,Dennin,Blondeau,Sliwa

, p. 1155 - 1156 (1990)

Novel purine isosters (title compounds) have been prepared by condensation of the appropriate o-hydroxyaminoazine with ethyl orthoformate; extension to other orthoesters and to benzyl thioacetimidate afford 2-alkyl substituted derivatives of these new fus

Syntheses of oxazolo[4,5-b]pyridenes and [4,5-d]pyrimidines

Doise,Blondeau,Sliwa

, p. 2891 - 2901 (1992)

Oxazolo[4,5-b]pyridines and [4,5-d]pyrimidines and their 2-substituted compounds have been prepared respectively by condensation of orthoesters of thioimidates derivatives with 2-amino-3-hydroxypyridine and 4-amino-5-hydroxypyrimidine.

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