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2-(3-bromophenyl)-2,2-difluoroethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

915133-40-3

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915133-40-3 Usage

Type of compound

Fluorinated alcohol

Bromophenyl group

Contains a 3-bromophenyl group in its structure

Usage in organic synthesis

Commonly used as a building block for the synthesis of various pharmaceuticals and agrochemicals

Usage as a reagent

Utilized in chemical reactions, such as the formation of carbon-carbon bonds and the preparation of fluorine-containing compounds

Potential applications

Has potential applications in the development of new materials

Field of interest

Of interest in the field of fluorine chemistry due to its unique properties

Check Digit Verification of cas no

The CAS Registry Mumber 915133-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,1,3 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 915133-40:
(8*9)+(7*1)+(6*5)+(5*1)+(4*3)+(3*3)+(2*4)+(1*0)=143
143 % 10 = 3
So 915133-40-3 is a valid CAS Registry Number.

915133-40-3Downstream Products

915133-40-3Relevant academic research and scientific papers

NOVEL BENZYLAMINO SUBSTITUTED QUINAZOLINES AND DERIVATIVES AS SOS1 INHIBITORS

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Page/Page column 95-96, (2018/07/29)

The present invention encompasses compounds of formula (I), wherein the groups R1 to R7 have the meanings given in the claims and specification, their use as inhibitors of SOS1, pharmaceutical compositions which contain compounds of this kind and their use as medicaments/medical uses, especially as agents for treatment and/or prevention of oncological diseases.

DERIVATIVES OF 4-(2-AMINO-1-HYDROXYETHYL)PHENOL AS AGONISTS OF THE β2 ADRENERGIC RECEPTOR

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Page/Page column 60, (2008/06/13)

The present invention provides a compound of formula (I) wherein: R1 is a group selected from -CH2OH, -NHC(O)H and R2 is a hydrogen atom; or R1 together with R2 form the group -NH-C(O)-CH=CH- wherein the nitrogen atom is bound to the carbon atom in the phenyl ring holding R1 and the carbon atom is bound to the carbon atom in the phenyl ring holding R2; R3 is selected from hydrogen and halogen atoms or groups selected from -SO-R5, -SO2- R5, -NH-CO-NH2, -CO-NH2, hydantoino, C1-4alkyl, C1-4alkoxy and -SO2NR5R6; R4 is selected from hydrogen atoms, halogen atoms and C1-4alkyl groups; R5 is a C1-4alkyl group or C3-8 cycloalkyl; R6 is independently selected from hydrogen atoms and C1-4alkyl groups; n, p and q are independently 0, 1 , 2, 3 or 4; m and s are independently 0, 1 , 2 or 3; r is 0, 1 or 2; with the provisos that: at least one of m and r is not 0; the sum n+m+p+q+r+s is 7, 8, 9, 10, 11 , 12 or 13; the sum q+r+s is 2, 3, 4, 5 or 6 or a pharmaceutically-acceptable salt, solvate or stereoisomer thereof.

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