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Oxazole, 2-(3-butylphenyl)-4,5-dihydro-4,4-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82946-70-1

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82946-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82946-70-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,4 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82946-70:
(7*8)+(6*2)+(5*9)+(4*4)+(3*6)+(2*7)+(1*0)=161
161 % 10 = 1
So 82946-70-1 is a valid CAS Registry Number.

82946-70-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-butylphenyl)-4,4-dimethyl-5H-1,3-oxazole

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:82946-70-1 SDS

82946-70-1Downstream Products

82946-70-1Relevant academic research and scientific papers

THE SYNTHESIS OF 1,2,3-TRISUBSTITUTED BENZENES. FURTHER COMMENTS ON BENZYNES DERIVED FROM ARYL OXAZOLINES

Meyers, A. I.,Pansegrau, Paul D.

, p. 4935 - 4938 (2007/10/02)

Further investigation of organolithium addition to the 2,3-benzyne of aryl oxazolines reveals that addition takes place to give the 3-lithio (kinetic) and/or 2-lithio (thermodynamic) products depending on the nature of the organolithium reagent.

BENZYNE DERIVED FROM ARYLOXAZOLINES. A VERSATILE INTERMEDIATE.

Meyers, A. I.,Rieker, William

, p. 2091 - 2094 (2007/10/02)

The benzyne derived from m-chlorophenyl oxazoline adds nucleophiles regiospecifically producing m-substituted products.Electrophiles are also trapped furnishing 1,2,3-trisubstituted benzenes.

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