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1-Isoropenylo-carborane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30619-60-4

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30619-60-4 Usage

Highly stable and non-toxic molecule

1-Isoropenylo-carborane (1-ICB) is a stable and non-toxic compound, making it a promising candidate for various applications in the field of materials science and biomedical research.

Potential use in cancer treatment

1-ICB has been investigated for its potential use in cancer treatment, as it may have properties that can be useful in targeting and destroying cancer cells.

Development of new types of polymers, ceramics, and metal complexes

1-ICB's unique chemical structure makes it an attractive option for the development of new types of materials, including polymers, ceramics, and metal complexes.

High thermal and chemical stability

The carbon cage structure of 1-ICB, which includes boron atoms and hydrogen, gives it a high level of thermal and chemical stability, making it suitable for a wide range of industrial and scientific applications.

Development of new types of catalytic systems

1-ICB has also been studied for its potential use in the development of new types of catalytic systems, which could have a wide range of industrial and scientific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 30619-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,1 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30619-60:
(7*3)+(6*0)+(5*6)+(4*1)+(3*9)+(2*6)+(1*0)=94
94 % 10 = 4
So 30619-60-4 is a valid CAS Registry Number.

30619-60-4Relevant articles and documents

Directive effects in the hydroboration of 1-alkenyl derivatives of o-carborane with representative hydroborating agents

Kabalka,Hondrogiannis

, p. 327 - 337 (1997)

A series of 1-alkenyl-o-carboranes was hydroborated using representative hydroborating agents with different steric requirements. The steric and electronic effects of the carboranyl group were evaluated by examining the distribution of the isomeric alcohols obtained after oxidation of the intermediate carboranyl-substituted organoboranes.

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