16706-54-0 Usage
Description
Carbamic acid, (aminoiminomethyl)-, phenylmethyl ester, also known as phenylmethyl carbamate, is a carbamate ester derived from carbamic acid and phenylmethyl alcohol. It is a chemical compound with a broad spectrum of activity against various pests, commonly used as a fungicide and insecticide in agriculture. Carbamic acid, being a weak acid, is also utilized in the synthesis of pharmaceuticals and agricultural chemicals. However, due to its potential toxicity to humans and the environment, proper handling and usage are crucial.
Uses
Used in Agricultural Industry:
Carbamic acid, (aminoiminomethyl)-, phenylmethyl ester is used as a fungicide and insecticide for controlling pests in agriculture. Its broad-spectrum activity makes it effective against a wide range of pests, helping to protect crops and ensure a stable food supply.
Used in Pharmaceutical Industry:
Carbamic acid, (aminoiminomethyl)-, phenylmethyl ester is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into the development of new drugs, potentially offering novel therapeutic options for various medical conditions.
Used in Chemical Synthesis:
Carbamic acid, (aminoiminomethyl)-, phenylmethyl ester is used as a versatile building block in the synthesis of a variety of chemical compounds. Its reactivity and functional groups make it a valuable component in the creation of new molecules with diverse applications in various industries, including agriculture, pharmaceuticals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 16706-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,0 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16706-54:
(7*1)+(6*6)+(5*7)+(4*0)+(3*6)+(2*5)+(1*4)=110
110 % 10 = 0
So 16706-54-0 is a valid CAS Registry Number.
16706-54-0Relevant articles and documents
A facile and efficient multi-gram synthesis of N-protected 5-(guanidinocarbonyl)-1H-pyrrole-2-carboxylic acids
Schmuck, Carsten,Bickert, Volker,Merschky, Michael,Geiger, Lars,Rupprecht, Daniel,Dudaczek, Juergen,Wich, Peter,Rehm, Thomas,Machon, Uwe
, p. 324 - 329 (2008/09/18)
The synthesis of two versatile building blocks for supramolecular anion binding motifs, 5-(N-Boc-guanidinocarbonyl)-1H-pyrrole-2-carboxylic acid (1) and 5-(N-Cbz-guanidinocarbonyl)-1H-pyrrole-2-carboxylic acid (2) is reported. Using these building blocks, a guanidiniocarbonyl-pyrrole anion binding site can easily be introduced into more complex molecules by using standard amide coupling conditions. Both syntheses can be performed on a multi-gram scale. The products are obtained in pure form and can be stored as solids without decomposition. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.
