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937372-03-7

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937372-03-7 Usage

General Description

CarbaMic acid, N-(3,4-diaMinophenyl)-, 1,1-diMethylethyl ester is a chemical compound with the molecular formula C14H19N3O3. It is commonly used as an intermediate in the synthesis of pharmaceutical compounds and dyes. CarbaMic acid, N-(3,4-diaMinophenyl)-, 1,1-diMethylethyl ester is a derivative of carbaMic acid and is typically found in the form of a white or off-white crystalline powder. It is important to handle this compound with care as it may cause skin and eye irritation upon contact. Additionally, it should be stored in a cool, dry place and kept away from sources of heat and flame. This chemical is used in various industrial and research applications, particularly in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 937372-03-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,7,3,7 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 937372-03:
(8*9)+(7*3)+(6*7)+(5*3)+(4*7)+(3*2)+(2*0)+(1*3)=187
187 % 10 = 7
So 937372-03-7 is a valid CAS Registry Number.
InChI:InChI=1S/C11H17N3O2/c1-11(2,3)16-10(15)14-7-4-5-8(12)9(13)6-7/h4-6H,12-13H2,1-3H3,(H,14,15)

937372-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(3,4-diaminophenyl)carbamate

1.2 Other means of identification

Product number -
Other names -

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:937372-03-7 SDS

937372-03-7Relevant articles and documents

Mechanochemical catalytic transfer hydrogenation of aromatic nitro derivatives

Portada, Tomislav,Margeti?, Davor,?trukil, Vjekoslav

supporting information, (2018/12/11)

Mechanochemical ball milling catalytic transfer hydrogenation (CTH) of aromatic nitro compounds using readily available and cheap ammonium formate as the hydrogen source is demonstrated as a simple, facile and clean approach for the synthesis of substituted anilines and selected pharmaceutically relevant compounds. The scope of mechanochemical CTH is broad, as the reduction conditions tolerate various functionalities, for example nitro, amino, hydroxy, carbonyl, amide, urea, amino acid and heterocyclic. The presented methodology was also successfully integrated with other types of chemical reactions previously carried out mechanochemically, such as amide bond formation by coupling amines with acyl chlorides or anhydrides and click-type coupling reactions between amines and iso(thio)cyanates. In this way, we showed that active pharmaceutical ingredients Procainamide and Paracetamol could be synthesized from the respective nitro-precursors on milligram and gram scale in excellent isolated yields.

Synthesis and chemical characterisation of target identification reagents based on an inhibitor of human cell invasion by the parasite Toxoplasma gondii

Evans, Kathryn M.,Haraldsen, Jeralyn D.,Pearson, Russell J.,Slawin, Alexandra M. Z.,Ward, Gary E.,Westwood, Nicholas J.

, p. 2063 - 2069 (2008/03/18)

The use of phenotype-based screens as an approach for identifying novel small molecule tools is reliant on successful protein target identification strategies. Here we report on the synthesis and chemical characterisation of a novel reagent for protein ta

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