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

96227-33-7

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96227-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96227-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,2,2 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 96227-33:
(7*9)+(6*6)+(5*2)+(4*2)+(3*7)+(2*3)+(1*3)=147
147 % 10 = 7
So 96227-33-7 is a valid CAS Registry Number.

96227-33-7SDS

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-(3-methoxy-5-methylphenyl)-4,4-dimethyl-5H-1,3-oxazole

1.2 Other means of identification

Product number -
Other names 2-(3-methoxy-5-methylphenyl)-4,4-dimethyl-2-oxazoline

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:96227-33-7 SDS

96227-33-7Relevant academic research and scientific papers

A New Synthesis of Defucogilvocarcin M

Hart, David J.,Merriman, Gregory H.

, p. 5093 - 5096 (2007/10/02)

A convergent synthesis of the title compound is described.The synthesis revolves around a MAD-mediated coupling of oxazoline 11 and naphthoquinone ketal 16 and requires eight steps via the longest linear sequence.

Synthesis of Antibiotic SS-228R. Strong Base Induced Cycloaddition of Homophthalic Anhydrides

Tamura, Yasumitsu,Fukata, Fumio,Sasho, Manabu,Tsugoshi, Teruhisa,Kita, Yasuyuki

, p. 2273 - 2277 (2007/10/02)

Two types of naphthacenediones, 1,6,7-trihydroxy-9-methyl- (2) and 1,6,10-trihydroxy-8-methyl-naphthacene-5,12-diones (4), were prepared by the cycloaddition of 8-methoxy-6-methyl- (9) and 5-methoxy-7-methylhomophthalic anhydrides (10) with 2-bromojuglone

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