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N-(2-N,N-dimethylaminophenyl)-1,1-dimethylethyl ester carbamic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

696604-98-5

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696604-98-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 696604-98-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,6,6,0 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 696604-98:
(8*6)+(7*9)+(6*6)+(5*6)+(4*0)+(3*4)+(2*9)+(1*8)=215
215 % 10 = 5
So 696604-98-5 is a valid CAS Registry Number.

696604-98-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-N,N-dimethylaminophenyl)-1,1-dimethylethyl ester carbamic acid

1.2 Other means of identification

Product number -
Other names N,N-dimethyl-N'-(tert-butyloxycarbonyl)-1,2-diaminobenzene

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:696604-98-5 SDS

696604-98-5Relevant academic research and scientific papers

Synthetic fosmidomycin analogues with altered chelating moieties do not inhibit 1-deoxy-d-xylulose 5-phosphate reductoisomerase or Plasmodium falciparum growth in vitro

Chofor, Rene,Risseeuw, Martijn D.P.,Pouyez, Jenny,Johny, Chinchu,Wouters, Johan,Dowd, Cynthia S.,Couch, Robin D.,Van Calenbergh, Serge

, p. 2571 - 2587 (2014/03/21)

Fourteen new fosmidomycin analogues with altered metal chelating groups were prepared and evaluated for inhibition of E. coli Dxr, M. tuberculosis Dxr and the growth of P. falciparum K1 in human erythrocytes. None of the synthesized compounds showed activ

Palladium-catalyzed coupling of ammonia with aryl chlorides, bromides, iodides, and sulfonates: A general method for the preparation of primary arylamines

Vo, Giang D.,Hartwig, John F.

supporting information; experimental part, p. 11049 - 11061 (2009/12/05)

We report that the complex generated from Pd[P(o-tol)3] 2 and the alkylbisphosphine CyPF-t-Bu is a highly active and selective catalyst for the coupling of ammonia with aryl chlorides, bromides, iodides, and sulfonates. The couplings of ammonia with this catalyst conducted with a solution of ammonia in dioxane form primary arylamines from a variety of aryl electrophiles in high yields. Catalyst loadings as low as 0.1 mol % were sufficient for reactions of many aryl chlorides and bromides. In the presence of this catalyst, aryl sulfonates also coupled with ammonia for the first time in high yields. A comparison of reactions in the presence of this catalyst versus those in the presence of existing copper and palladium systems revealed a complementary, if not broader, substrate scope. The utility of this method to generate amides, imides, and carbamates is illustrated by a one-pot synthesis of a small library of these carbonyl compounds from aryl bromides and chlorides, ammonia, and acid chlorides or anhydrides. Mechanistic studies show that reactions conducted with the combination of Pd[P(o-tol)3]2 and CyPF-t-Bu as catalyst occur with faster rates and higher yields than those conducted with CyPF-t-Bu and palladiun(II) as catalyst precursors because of the low concentration of active catalyst that is generated from the combination of palladium(II), ammonia, and base.

Design and synthesis of a novel family of semi-rigid ligands: Versatile compounds for the preparation of 99mTc radiopharmaceuticals

Le Gal, Julien,Latapie, Laure,Gressier, Marie,Coulais, Yvon,Dartiguenave, Michele,Benoist, Eric

, p. 876 - 883 (2007/10/03)

Synthetic pathways to a range of novel semi-rigid tetradentate ligands, with sulfur, amido or amino donor groups, designed to coordinate technetium 99m have been developed. The technetium-99m complexes have been prepared and their stabilities in serum and

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