676464-98-5 Usage
Uses
Used in Organic Synthesis:
Carbamic acid, [3-(ethylamino)-4-pyridinyl]-, 1,1-dimethylethyl ester (9CI) is used as a reagent in organic synthesis for its ability to act as a protective group for amines. This allows chemists to carry out reactions without affecting the amine functionality, which can be crucial for the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Carbamic acid, [3-(ethylamino)-4-pyridinyl]-, 1,1-dimethylethyl ester (9CI) is utilized in the synthesis of various drug molecules. Its role as a protective group for amines enables the development of new drugs with specific properties and improved therapeutic effects.
Used in Chemical Research:
Carbamic acid, [3-(ethylamino)-4-pyridinyl]-, 1,1-dimethylethyl ester (9CI) is also used in chemical research to study the reactivity and properties of amines. Researchers can use Carbamic acid,[3-(ethylamino)-4-pyridinyl]-,1,1-dimethylethyl ester (9CI) to explore new reaction pathways and develop innovative synthetic methods.
Safety Precautions:
It is important to handle Carbamic acid, [3-(ethylamino)-4-pyridinyl]-, 1,1-dimethylethyl ester (9CI) with care, as it can be harmful if inhaled, ingested, or comes into contact with the skin. Proper safety precautions and handling procedures should be followed when working with this chemical to avoid any potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 676464-98-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,6,4,6 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 676464-98:
(8*6)+(7*7)+(6*6)+(5*4)+(4*6)+(3*4)+(2*9)+(1*8)=215
215 % 10 = 5
So 676464-98-5 is a valid CAS Registry Number.
676464-98-5Relevant articles and documents
Regioselective synthesis of an imidazo[4,5-c]pyridine through selective acylation of 3,4-diaminopyridine: Synthesis of CP-885,316
Caron, Stephane,Do, Nga M.,McDermott, Ruth E.,Bahmanyar
, p. 257 - 261 (2012/12/22)
CP-885,316 (1), an imidazo[4,5-c]pyridine, 4, was prepared from 3,4-diaminopyridine (9). Two routes were demonstrated using the regioselective introduction of either an acetamide at the 3-position or a tert-butylcarbamate at the 4-position.
Process for preparing haloalkyl pyrimidines
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Page 5, (2008/06/13)
The invention is a process for producing haloalkyl pyrimidines as intermediates in the production of benzimidazole and/or pyridylimidazole derivatives having high selectivity and/or high affinity to the benzodiazepine site of GABAA receptors.
