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94330-95-7

94330-95-7

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94330-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94330-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,3 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94330-95:
(7*9)+(6*4)+(5*3)+(4*3)+(3*0)+(2*9)+(1*5)=137
137 % 10 = 7
So 94330-95-7 is a valid CAS Registry Number.

94330-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-5-(3-phenyl-4,5-dihydro-1,2-oxazol-5-yl)-1,2-oxazole

1.2 Other means of identification

Product number -
Other names 5,5'-Biisoxazole,4,5-dihydro-3,3'-diphenyl

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:94330-95-7 SDS

94330-95-7Downstream Products

94330-95-7Relevant articles and documents

5-Hydroxy-3-phenyl-5-vinyl-2-isoxazoline and 3-phenyl-5-vinylisoxazole: Synthesis and reactivity

Di Nunno, Leonardo,Scilimati, Antonio,Vitale, Paola

, p. 11270 - 11278 (2007/10/03)

5-Hydroxy-3-phenyl-5-vinyl-2-isoxazoline has been synthesized by reacting benzonitrile oxide with the enolate ion of methyl vinyl ketone. From 5-hydroxy-5-vinyl-2-isoxazoline, 5-vinylisoxazole was then quantitatively obtained by dehydration-aromatization

REACTION DES METHYLENE γ-BUTYROLACTONES AVEC LES ARYLNITRILOXYDES. EVOLUTION INATTENDUE DU BIS ADDUIT ISSU DE LA 5-METHYLENE(5H)FURAN-2-ONE

Fihi, Rachid,Ciamala, Kabula,Vebrel, Joel,Rodier, Noel

, p. 55 - 62 (2007/10/02)

In explorations of synthesis and chemistry of spiroheterocycles, we found that reaction of aromatic nitrile oxydes with methylene γ-butyrolactones (at room temperature) produced spiroheterocycles 4,5 and 6.When cycloadditions were carried out in refluxing

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