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1-Naphthalenecarboxamide, N-(benzoyloxy)-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

194494-50-3

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194494-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194494-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,4,9 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 194494-50:
(8*1)+(7*9)+(6*4)+(5*4)+(4*9)+(3*4)+(2*5)+(1*0)=173
173 % 10 = 3
So 194494-50-3 is a valid CAS Registry Number.

194494-50-3SDS

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 N-(1-naphthoyl)-N-phenyl-O-benzoylhydroxylamine

1.2 Other means of identification

Product number -
Other names O-benzoyl-N-(1-naphthoyl)-N-phenylhydroxylamine

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:194494-50-3 SDS

194494-50-3Relevant academic research and scientific papers

Kinetic resolution of primary 2-methyl-substituted alcohols via Pseudomonas cepacia lipase-catalysed enantioselective acylation

Nordin, Ove,Nguyen, Ba-Vu,Voerde, Carin,Hedenstroem, Erik,Hoegberg, Hans-Erik

, p. 367 - 376 (2007/10/03)

The enantioselectivities of lipases from Pseudomonas cepacia (PFL, Amano PS, etc.) towards a series of primary 2-methyl-substituted alcohols using vinyl acetate as the acyl donor in transesterifications in organic solvents were studied. In terms of enantioselectivity, the best results were found for 3-aryl-2-methylpropan-1-ols with enantiomeric ratios (E-values) over 100 in most cases, whereas other 3-substituted primary 2-methylpropan-1-ols generally displayed lower enantioselectivities: 3-cycloalkyl-2-methylpropan-1-ols (E ≈ 20) and 2-methylalkan-1-ols (E ≈ 10). Moving the aryl group closer or further away from the chiral centre resulted in low enantioselectivities: 2-arylpropan-1-ols (E 10), 2-methyl-4-(2-thienyl)butan-1-ol (E = 12), 2-methyl-5-(2-thienyl)pentan-1-ol (E = 3.2) and 2-methyl-6-(2-thienyl)hexan-1-ol (E = 3.8).

Anionic Micellar Effects on the Benzophenone-sensitized Photolysis of N-(1-Naphthoyl)-N-phenyl-O-benzoylhydroxylamine

Kaneko, Tsuyoshi,Kubo, Kanji,Sakurai, Tadamitsu

, p. 2757 - 2774 (2007/10/03)

Most important property of compartmentalized liquids such as micelles is that they have an ability to concentrate guest molecules into relatively small effective volumes and then to promote the re-encounter of such molecules. This property also makes mice

Mechanism of the benzophenone-sensitized photolysis of O-benzoyl-N-(1- naphthoyl)-N-phenylhydroxylamine in cationic micellar media

Kaneko, Tsuyoshi,Tokue, Tatsuya,Kubo, Kanji,Sakurai, Tadamitsu

, p. 2771 - 2780 (2007/10/03)

The benzophenone-sensitized photolysis of the title hydroxylamine (1) in hexadecyltrimethylammonium chloride (HTAC) micelles was found to give benzoyloxy(2,3)- and phenyl(4,5)-migrated products, along with fragmentation products, 1-naphthanilide (6) and b

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