78469-86-0 Usage
Uses
Used in Pharmaceutical Industry:
(2R,3S)-(+)-3-(BENZYLOXYMETHYL)OXIRANE-2-METHANOL 4-NITROBENZOIC ACID ESTER is used as a building block in organic synthesis for the development of new pharmaceuticals. Its unique structure allows for the creation of novel drug candidates with potential therapeutic benefits.
Used in Agrochemical Industry:
In the agrochemical industry, (2R,3S)-(+)-3-(BENZYLOXYMETHYL)OXIRANE-2-METHANOL 4-NITROBENZOIC ACID ESTER is used as a precursor for the synthesis of new agrochemicals, potentially leading to the development of innovative products for crop protection and enhancement.
Used in Industrial Material Production:
(2R,3S)-(+)-3-(BENZYLOXYMETHYL)OXIRANE-2-METHANOL 4-NITROBENZOIC ACID ESTER is utilized as a component in the production of various industrial materials, where its unique properties can contribute to the development of advanced materials with specific applications.
Used in Chemical Reactions:
(2R,3S)-(+)-3-(BENZYLOXYMETHYL)OXIRANE-2-METHANOL 4-NITROBENZOIC ACID ESTER is also used in chemical reactions as a reactive intermediate, allowing for the synthesis of other complex organic molecules with potential applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 78469-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,6 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78469-86:
(7*7)+(6*8)+(5*4)+(4*6)+(3*9)+(2*8)+(1*6)=190
190 % 10 = 0
So 78469-86-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H17NO6/c20-18(14-6-8-15(9-7-14)19(21)22)24-12-17-16(25-17)11-23-10-13-4-2-1-3-5-13/h1-9,16-17H,10-12H2/t16-,17+/m0/s1
78469-86-0Relevant academic research and scientific papers
Chiral Electrophilic Synthetic Building Blocks with Four Different Functional Groups from Tartaric Acid, 2,3- and 3,4-Epoxy-butanediol Derivatives in All Four Stereoisomeric Forms
Hungerbuehler, Ernst,Seebach, Dieter
, p. 687 - 702 (2007/10/02)
Efficient and simple procedures have been developed for the preparation of the threo- and erythro-3,4-epoxy-1,2-butanediol derivatives 7 and 9 in both enantiomeric forms from tartaric acid.These epoxides should prove versatile as alkylating reagents in sy
