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(Z)-2-Amino-5-chlorobenzophenone oxime is an organic compound with the chemical formula C13H10ClNO and a molecular weight of 233.68 g/mol. It is a derivative of benzophenone, featuring a chlorine atom at the 5th position, an amino group at the 2nd position, and an oxime functional group. (Z)-2-Amino-5-chlorobenzophenone oxime is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides and drugs. It is characterized by its light-sensitive nature and is often used in the preparation of dyes and pigments due to its ability to form colored compounds. The (Z) configuration indicates the geometric isomerism around the double bond, which is crucial for its chemical properties and reactivity.

5013-10-5

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5013-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5013-10-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,1 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5013-10:
(6*5)+(5*0)+(4*1)+(3*3)+(2*1)+(1*0)=45
45 % 10 = 5
So 5013-10-5 is a valid CAS Registry Number.

5013-10-5SDS

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 2-amino-5-chlorobenzophenone α-oxime-(z)

1.2 Other means of identification

Product number -
Other names (Z)-2-Amino-5-chlorbenzophenonoxim

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:5013-10-5 SDS

5013-10-5Relevant academic research and scientific papers

A practical, metal-free synthesis of 1H-Lndazoles

Counceller, Carla M.,Eichman, Chad C.,Wray, Brertda C.,Stambuli, James P.

supporting information; experimental part, p. 1021 - 1023 (2009/04/07)

The synthesis of 1H-indazoles is achieved from o-aminobenzoximes by the selective activation of the oxime in the presence of the amino group. The reaction occurs with a variety of substituted o-aminobenzoximes using a slight excess of methanesulfonyl chloride and triethylamine at 0-23 °C and is amenable to scale-up. The synthesis of 1 H-indazoles under these conditions is extremely mild compared with previous synthetic approaches and affords the desired compounds in good to excellent yields.

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