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Benzenecarboximidamide, N-phenyl, monohydrochloride (9CI) is a chemical compound with the molecular formula C13H12ClN3. It is a derivative of benzenecarboximidamide, where a phenyl group is attached to the nitrogen atom, and a hydrochloride ion is present. Benzenecarboximidamide,N-phenyl-, monohydrochloride (9CI) is also known as N-phenylbenzenecarboximidamide hydrochloride or N-phenylbenzenecarboximidic acid hydrochloride. It is a white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. The compound is soluble in water and has a melting point of around 200-202°C. It is important to handle this chemical with care due to its potential toxicity and reactivity.

305-30-6

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305-30-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 305-30-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 305-30:
(5*3)+(4*0)+(3*5)+(2*3)+(1*0)=36
36 % 10 = 6
So 305-30-6 is a valid CAS Registry Number.

305-30-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-phenylbenzenecarboximidamide,hydrochloride

1.2 Other means of identification

Product number -
Other names N-phenyl-benzamidine,hydrochloride

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:305-30-6 SDS

305-30-6Relevant academic research and scientific papers

Synthesis of N-substituted aryl amidines by strong base activation of amines

Khalifa, Muhammad M.,Bodner, Micah J.,Berglund, J. Andrew,Haley, Michael M.

, p. 4109 - 4111 (2015)

Abstract We describe an efficient method for the direct preparation of N-substituted aryl amidines from nitriles and primary amines. The protocol employs activation of amines by a strong base and provides greater access to a pharmaceutically relevant functional group. This synthetic approach tolerates deactivated nitriles, nitriles with competing substitution sites, and aryl amines.

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