75148-49-1 Usage
Description
3-Bromobenzaldehyde diethyl acetal is an acetal derivative of 3-bromobenzaldehyde, characterized by its clear colorless liquid appearance. It is a chemical compound that holds potential applications in various industries due to its unique properties.
Uses
Used in Chemical Synthesis:
3-Bromobenzaldehyde diethyl acetal is used as an intermediate in the synthesis of various organic compounds. Its ability to undergo specific chemical reactions makes it a valuable component in the preparation of complex molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Bromobenzaldehyde diethyl acetal is used as a key building block for the development of new drugs. Its unique chemical structure allows for the creation of novel therapeutic agents that can target specific biological pathways.
Used in Material Science:
3-Bromobenzaldehyde diethyl acetal may also find applications in the field of material science, where it can be utilized to develop new materials with specific properties. Its chemical versatility enables it to be a part of innovative material formulations.
Specific Application:
3-Bromobenzaldehyde diethyl acetal is used in the preparation of 3-(tris[2-perfluorohexylethyl]stannyl)benzaldehyde, which is an important compound in the field of organic chemistry. This application highlights the compound's role in creating specialized chemical entities for various purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 75148-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,4 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75148-49:
(7*7)+(6*5)+(5*1)+(4*4)+(3*8)+(2*4)+(1*9)=141
141 % 10 = 1
So 75148-49-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H15BrO2/c1-3-13-11(14-4-2)9-6-5-7-10(12)8-9/h5-8,11H,3-4H2,1-2H3
75148-49-1Relevant articles and documents
Practical acetalization and transacetalization of carbonyl compounds catalyzed by recyclable PVP-I
Cao, Fu-Rong,Lu, Guangying,Ren, Jiangmeng,Wang, Di,Zeng, Bu-Bing
, (2021/06/21)
A novel PVP-I catalyzed acetalizations/transacetalizations of carbonyl compounds has been developed processing with a mild and easy handling fashion. Different types of Acyclic and cyclic acetals were prepared from carbonyl compounds or their acetals successfully. Further applications of newly developed catalytic combination were testified. This protocol featured with simplicity of operation, mild reaction condition, short reaction time, recyclable of catalyst and broad substrates scope with excellent yields.
Triarylborane-dipyrromethane conjugates bearing dual receptor sites: The synthesis and evaluation of the anion binding site preference
Swamy P., Chinna Ayya,Priyanka, Ragam N.,Thilagar, Pakkirisamy
, p. 4067 - 4075 (2014/03/21)
The synthesis and optical properties of four new triarylborane- dipyrromethane (TAB-DPM) conjugates (3a-d) containing dual binding sites (hydrogen bond donor and Lewis acid) have been reported. The new compounds exhibit a selective fluorogenic response towards the F- ion. The NMR titrations show that the anions bind to the TAB-DPM conjugates via the Lewis acidic triarylborane centre in preference to the hydrogen bond donor (dipyrromethane) units.
Gallium triiodide as a highly efficient and mild catalyst for the diethyl acetalization of carbonyl compounds
Ding, Jin-Chang,Xu, Rong,Liu, Miao-Chang,Chen, Xi-An,Wu, Hua-Yue
experimental part, p. 566 - 568 (2009/07/18)
Diethyl acetals were obtained from carbonyl compounds in good to excellent yields under mild reaction conditions in the presence of triethyl orthoformate and a catalytic amount of gallium triiodide in anhydrous ethanol.
