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443331-14-4

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443331-14-4 Usage

General Description

"(4-aminomethyl-phenyl)-carbamic acid benzyl ester" is a chemical compound that consists of a benzyl ester of (4-aminomethyl-phenyl)-carbamic acid. (4-AMINOMETHYL-PHENYL)-CARBAMIC ACID BENZYL ESTER is used in organic synthesis and pharmaceutical research as a building block for the synthesis of various biologically active molecules. It has potential applications in the development of new drugs and medicines due to its ability to interact with biological targets and receptors. The chemical structure and properties of this compound make it a valuable tool for researchers and scientists in the field of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 443331-14-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,3,3 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 443331-14:
(8*4)+(7*4)+(6*3)+(5*3)+(4*3)+(3*1)+(2*1)+(1*4)=114
114 % 10 = 4
So 443331-14-4 is a valid CAS Registry Number.

443331-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl N-[4-(aminomethyl)phenyl]carbamate

1.2 Other means of identification

Product number -
Other names benzyl 4-(aminomethyl)phenylcarbamate

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:443331-14-4 SDS

443331-14-4Relevant articles and documents

A method for the selective protection of aromatic amines in the presence of aliphatic amines

Perron, Valerie,Abbott, Shaun,Moreau, Nancie,Lee, Devin,Penney, Christopher,Zacharie, Boulos

experimental part, p. 283 - 289 (2009/06/25)

A simple and efficient procedure has been developed for the regioselective protection of aromatic amines in the presence of aliphatic amines. The method is general for the preparation of mono-N-Boc, -N-Cbz, -N-Fmoc or -N-Alloc aromatic amines in high yield without affecting the aliphatic amines. This approach is applicable to substituted (aminoalkyl)aniline compounds with different functionalities and was employed to supply gram quantities of the protected aniline product. Georg Thieme Verlag Stuttgart · New York.

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