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Tert-Butyl 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate is a complex organic compound that falls under the category of boronic acids and esters. It is characterized by the presence of a boronic acid or ester, which is a compound containing a boron atom bonded to three hydroxyl groups or an ester formed by the condensation of these acids with an alcohol. tert-Butyl 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate is notable for its multiple functional groups, including a tert-butyl group, a methyl group, phenyl rings, a carbamate group, and a 1,3,2-dioxaborolane group. The inclusion of a boronic ester suggests its potential utility in cross-coupling reactions and other applications within organic synthesis. The synthesis of tert-Butyl 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate demands meticulous control over reaction conditions due to its intricate structure.

1256360-04-9

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1256360-04-9 Usage

Uses

Used in Chemical Synthesis:
Tert-Butyl 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate is used as a synthetic intermediate for the preparation of various complex organic molecules. Its boronic ester functionality allows it to participate in cross-coupling reactions, which are pivotal in constructing carbon-carbon bonds in organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, tert-Butyl 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate is used as a building block for the synthesis of potential drug candidates. Its unique structure and reactivity can be harnessed to create novel compounds with therapeutic potential.
Used in Material Science:
Tert-Butyl 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate is used as a component in the development of new materials with specific properties. Its versatility in organic synthesis can lead to the creation of materials with tailored characteristics for various applications, such as in electronics or as specialty coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 1256360-04-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,6 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1256360-04:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*6)+(3*0)+(2*0)+(1*4)=139
139 % 10 = 9
So 1256360-04-9 is a valid CAS Registry Number.

1256360-04-9Relevant academic research and scientific papers

SYSTEM FOR FORMING AN ELECTROACTIVE LAYER

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Paragraph 0362; 0363, (2016/11/14)

There is provided an electroactive system for forming an electroactive layer. The system includes: (a) a first electroactive material; (b) a facilitation additive; and (c) a first liquid medium. The facilitation additive is present during baking in an amo

SOLVENT-RESISTANT HOLE TRANSPORT LAYERS

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, (2015/06/25)

There is provided a hole transport material having Formula I, Formula Ia, or Formula II: In the formulae: A is an aromatic moiety including at least one triarylamino group; B' is an aromatic moiety; E is an end group which is H, D, alkyl, aryl, halide, de

ELECTROACTIVE MATERIALS

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, (2012/01/06)

There is disclosed a compound having Formula I or Formula I': In Formula I and Formula I': Ar1 and Ar2 are the same or different and are aryl groups; R1 through R5 are independently the same or different at each occurrence and are D, F, alkyl groups, aryl groups, alkoxy groups, silyl groups, or crosslinkable groups; R6 is H, D, or halogen; a through e are independently an integer from 0 to 4; f is 1 or 2; g is 0, 1 or 2; h is 1 or 2; and n is an integer greater than 0.

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