85232-02-6 Usage
Uses
Used in Organic Synthesis:
N-(TERT-BUTOXYCARBONYL)PHOSPHORAMIDIC ACID DIETHYL ESTER serves as a valuable reagent in organic synthesis, facilitating the formation of complex organic molecules and contributing to the advancement of chemical research.
Used in Peptide Synthesis:
In the field of peptide synthesis, N-(TERT-BUTOXYCARBONYL)PHOSPHORAMIDIC ACID DIETHYL ESTER is employed as a protecting group for amino acids. This function is crucial for preventing unwanted side reactions during the assembly of peptide chains, ensuring the successful synthesis of desired peptide sequences.
Used in Pharmaceutical Synthesis:
N-(TERT-BUTOXYCARBONYL)PHOSPHORAMIDIC ACID DIETHYL ESTER acts as a building block in the synthesis of pharmaceuticals. Its incorporation into drug molecules can lead to the development of new medications with improved efficacy and reduced side effects.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical industry, N-(TERT-BUTOXYCARBONYL)PHOSPHORAMIDIC ACID DIETHYL ESTER is used as a key component in the synthesis of various agrochemicals. This contributes to the creation of innovative products for agricultural applications, such as pesticides and herbicides, to enhance crop protection and yield.
Used in Organic Chemistry Laboratories:
Due to its stability and ease of handling, N-(TERT-BUTOXYCARBONYL)PHOSPHORAMIDIC ACID DIETHYL ESTER is a popular compound in organic chemistry laboratories. It is frequently used in teaching and research settings to demonstrate various chemical principles and reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 85232-02-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,3 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 85232-02:
(7*8)+(6*5)+(5*2)+(4*3)+(3*2)+(2*0)+(1*2)=116
116 % 10 = 6
So 85232-02-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H20NO5P/c1-6-13-16(12,14-7-2)10-8(11)15-9(3,4)5/h6-7H2,1-5H3,(H,10,11,12)
85232-02-6Relevant articles and documents
A new access to substituted tetraethyl N-Boc 2-aminoethylidene-1,1-bisphosphonates and phosphonyl-substituted aza-Morita-Baylis-Hillman-type adducts
Gajda, Anna,Gajda, Tadeusz
, p. 1233 - 1241 (2008/09/17)
A general one-pot synthesis of substituted 2-aminoethylidene-1,1-bisphosphonates has been developed. The protocol involves base-induced addition of sodium tetraethyl methylenebisphosphonate to N-Boc imines generated in situ from N-Boc-α-amidoalkyl-p-tolyl