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3-(tert-butyl)-5-formyl-4-hydroxybenzoic acid is a complex organic compound with the molecular formula C11H12O4. It is characterized by a benzoic acid structure, where the 3-position is occupied by a tert-butyl group, the 5-position has a formyl group (an aldehyde), and the 4-position contains a hydroxyl group. This chemical is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique functional groups, which can participate in various chemical reactions. The presence of the tert-butyl group provides steric hindrance, while the formyl and hydroxyl groups offer sites for further chemical modification, making it a versatile building block in organic synthesis.

882500-52-9

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882500-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 882500-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,5,0 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 882500-52:
(8*8)+(7*8)+(6*2)+(5*5)+(4*0)+(3*0)+(2*5)+(1*2)=169
169 % 10 = 9
So 882500-52-9 is a valid CAS Registry Number.

882500-52-9Relevant academic research and scientific papers

Controlled Exchange of Achiral Linkers with Chiral Linkers in Zr-Based UiO-68 Metal-Organic Framework

Tan, Chunxia,Han, Xing,Li, Zijian,Liu, Yan,Cui, Yong

supporting information, p. 16229 - 16236 (2018/11/27)

The development of highly robust heterogeneous catalysts for broad asymmetric reactions has always been a subject of interest, but it remains a synthetic challenge. Here we demonstrated that highly stable metal-organic frameworks (MOFs) with potentially acid-labile chiral catalysts can be synthesized via postsynthetic exchange. Through a one- or two-step ligand exchange, a series of asymmetric metallosalen catalysts with the same or different metal centers are incorporated into a Zr-based UiO-68 MOF to form single- and mixed-M(salen) linker crystals, which cannot be accomplished by direct solvothermal synthesis. The resulting MOFs have been characterized by a variety of techniques including single-crystal X-ray diffraction, N2 sorption, CD, and SEM/TEM-EDS mapping. The single-M(salen) linker MOFs are active and efficient catalysts for asymmetric cyanosilylation of aldehydes, ring-opening of epoxides, oxidative kinetic resolution of secondary alcohols, and aminolysis of stilbene oxide, and the mixed-M(salen) linker variants are active for sequential asymmetric alkene epoxidation/epoxide ring-opening reactions. The chiral MOF catalysts are highly enantioselective and completely heterogeneous and recyclable, making them attractive catalysts for eco-friendly synthesis of fine chemicals. This work not only advances UiO-type MOFs as a new platform for heterogeneous asymmetric catalysis in a variety of syntheses but also provides an attractive strategy for designing robust and versatile heterogeneous catalysts.

Nano- and microcrystals of a Mn-based metal-oligomer framework showing size-dependent magnetic resonance behaviors

Yuan, Guozan,Zhu, Chengfeng,Liu, Yan,Cui, Yong

, p. 3180 - 3182 (2011/05/07)

A robust 3D Mn-based metal-organic framework containing metallosalen hexamers is synthesized and its nano- and microcrystals are fabricated by using surfactant-mediated hydrothermal and solvent precipitation methods; the particles exhibit an inverse size-

Isoreticular chiral metal-organic frameworks for asymmetric alkene epoxidation: Tuning catalytic activity by controlling framework catenation and varying open channel sizes

Song, Feijie,Wang, Cheng,Falkowski, Joseph M.,Ma, Liqing,Lin, Wenbin

supporting information; experimental part, p. 15390 - 15398 (2011/01/10)

A family of isoreticular chiral metal-organic frameworks (CMOFs) of the primitive cubic network topology was constructed from [Zn4(μ 4-O)(O2CR)6] secondary building units and systematically elongated dicarboxyla

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