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2-ISOPROPYL-4,4-DIMETHYL-4,5-DIHYDRO-1,3-OXAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34575-25-2

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34575-25-2 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 38, p. 2129, 1973 DOI: 10.1021/jo00952a004

Check Digit Verification of cas no

The CAS Registry Mumber 34575-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,7 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34575-25:
(7*3)+(6*4)+(5*5)+(4*7)+(3*5)+(2*2)+(1*5)=122
122 % 10 = 2
So 34575-25-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO/c1-6(2)7-9-8(3,4)5-10-7/h6H,5H2,1-4H3

34575-25-2SDS

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 4,4-dimethyl-2-propan-2-yl-5H-1,3-oxazole

1.2 Other means of identification

Product number -
Other names 4,4-dimethyl-2-isopropyl-4,5-dihydrooxazole

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:34575-25-2 SDS

34575-25-2Relevant academic research and scientific papers

New Synthesis of Optically Active 5-Isoxazolidinones and β-Amino Acids

Luisi, Renzo,Capriati, Vito,Florio, Saverio,Vista, Teresa

, p. 9861 - 9864 (2007/10/03)

A new simple and stereoselective synthesis of 5-isoxazolidinones based on the reaction of lithiated 2-isopropyl-2-oxazolines with nitrones is described. A chiral version of such a methodology allows the preparation of highly enantioenriched 5-isoxazolidinones which are useful precursors for the synthesis of β-amino acids.

Alkyl Nitrate Nitration of Active Methylene Compounds. Nitration of 2-Substituted 2-Oxazolines

Feuer, Henry,Bevinakatti, Hanamanthsa S.,Luo, Xuan-Gan

, p. 825 - 832 (2007/10/02)

2-Alkyl- and 2-aralkyl-2-oxazolines are readily converted to the corresponding α-nitroalkyl- and α-nitroaralkyl-2-oxazolines an treatment with an alkali metal amide such as potassium or sodium amide in liquid ammonia or with lithium diisopropylamide (LDA)

SYNTHESIS OF ISOTHIOCYANATES FROM NON-AROMATIC NITROGEN-CONTAINING HETEROCYCLES

Gonda, Jozef,Kristian, Pavol,Mikler, Lubomir

, p. 112 - 117 (2007/10/02)

Investigation of the reaction of thiophosgene with Δ2-oxazolines I, Δ3-thiazolines II, 4H-benzothiazines III, 2-methoxypentahydro-Δ1-azepine IV, theophylline and caffeine showed that only compounds I and IV reacted to give 2-acyloxyethyl isothiocyanates and methyl 6-isothiocyanatohexanoate.The structure of these products was corroborated by IR, 1H NMR, 13C NMR and mass spectral methods.The suitability of the above-mentioned compounds to react is discussed.

Allenes. Part 44. Formation of Oxazolines and Benzoxazoles from Allenic nitriles and amides and from Phenylpropynenitrile.

Fomum, Z. Tanee,Nkengfack, A. Ephrem,Mpango, George W. P.,Landor, Stephen R.,Landor, Phyllis D.

, p. 901 - 924 (2007/10/02)

Michael addition of ethanolamines and 2-aminophenol to allenic nitriles, allenic amides and phenylpropynenitrile gives enaminic nitriles and amides which at 290 deg - 320 deg yield oxazolines and benzoxazoles.

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