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1073354-57-0

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1073354-57-0 Usage

General Description

TRANS-2-(3-CYCLOPENTYLPROPEN-1-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE is a compound with a complex structure, consisting of a cyclopentylpropenyl group and a dioxaborolane ring. The chemical contains four methyl groups attached to the dioxaborolane ring. TRANS-2-(3-CYCLOPENTYLPROPEN-1-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE is likely to have applications in organic synthesis, as dioxaborolanes are often used as reagents in various reactions, such as Suzuki coupling and other cross-coupling reactions. Its unique structure and properties may make it useful in the development of new materials or pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 1073354-57-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,3,5 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1073354-57:
(9*1)+(8*0)+(7*7)+(6*3)+(5*3)+(4*5)+(3*4)+(2*5)+(1*7)=140
140 % 10 = 0
So 1073354-57-0 is a valid CAS Registry Number.

1073354-57-0Relevant articles and documents

THERAPEUTIC COMPOUNDS AND METHODS OF USE

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Paragraph 0598; 0599; 0600, (2021/05/21)

The invention relates to compounds and methods of using said compounds, as well as pharmaceutical compositions containing such compounds, for treating diseases and conditions mediated by TEAD, such as cancer.

Rhodium-catalyzed dehydrogenative borylation of aliphatic terminal alkenes with pinacolborane

Morimoto, Masao,Miura, Tomoya,Murakami, Masahiro

supporting information, p. 12659 - 12663 (2015/10/28)

Aliphatic terminal alkenes react with pinacolborane at ambient temperature to afford dehydrogenative borylation compounds as the major product when iPr-Foxap is used as the ligand with cationic rhodium(I) in the presence of norbornene, which acts as the s

Efficient synthesis of diborylalkenes from alkenes and diboron by a new PSiP-pincer palladium-catalyzed dehydrogenative borylation

Takaya, Jun,Kirai, Naohiro,Iwasawa, Nobuharu

supporting information; experimental part, p. 12980 - 12983 (2011/10/04)

The efficient synthesis of various diborylalkenes such as 1,1-, trans-1,2-, and cyclic 1,2-diborylalkenes from alkenes and diboron was achieved for the first time. Selective preparation of di- and monoborylalkenes was also realized by the appropriate choi

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