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15185-37-2

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15185-37-2 Usage

General Description

(E)-2-Aminobenzophenone oxime is a chemical compound that belongs to the oxime family. It is an organic compound with the molecular formula C13H11NO and a molar mass of 197.23 g/mol. (E)-2-Aminobenzophenone oxime is used in various industrial applications, particularly as a photoinitiator in the production of photopolymers and as a stabilizer in the synthesis of various materials. It is also utilized as a reagent in organic synthesis, specifically in the formation of Schiff bases and in the preparation of heterocyclic compounds. Additionally, (E)-2-Aminobenzophenone oxime has potential applications in the pharmaceutical industry, particularly in the development of new drug compounds due to its unique chemical properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 15185-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,8 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15185-37:
(7*1)+(6*5)+(5*1)+(4*8)+(3*5)+(2*3)+(1*7)=102
102 % 10 = 2
So 15185-37-2 is a valid CAS Registry Number.

15185-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (NE)-N-[(2-aminophenyl)-phenylmethylidene]hydroxylamine

1.2 Other means of identification

Product number -
Other names 2-[(E)-(Hydroxyimino)(Phenyl)Methyl]Aniline

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:15185-37-2 SDS

15185-37-2Relevant articles and documents

Mild method for the synthesis of 1H-indazoles through oxime-phosphonium ion intermediate

Paul, Saurav,Panda, Subhankar,Manna, Debasis

supporting information, p. 2480 - 2483 (2014/05/06)

The synthesis of 1H-indazoles from o-aminobenzoximes is achieved via N-N bond formation using triphenylphosphine, I2, and imidazole. Selective formation of oxime-phosphonium ion intermediate in the presence of the amino group is the driving for

Quinazolines and 1,4-benzodiazepines. XXVI. 1,2-Dihydroquinazoline 3-oxides.

Field,Zally,Sternbach

, p. 3957 - 3959 (2007/10/06)

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