90470-67-0 Usage
1-(Dimethoxymethyl)-2-fluorobenzene
A benzene ring with a fluorine atom at the 2nd position and a methoxymethyl group attached to the 1st position.
1-(Dimethoxymethyl)-2-fluorobenzene
Contains a fluorine atom, a methoxymethyl group, and a benzene ring.
alpha,alpha-Dimethoxy-2-fluorotoluene
A toluene ring with a fluorine atom at the 2nd position and two methoxy groups attached to the alpha carbon.
alpha,alpha-Dimethoxy-2-fluorotoluene
Contains a fluorine atom, two methoxy groups, and a toluene ring.
Aromatic Compounds
Both compounds are aromatic, meaning they contain a benzene ring with delocalized pi electrons.
Applications
Both compounds are used in organic synthesis and have potential applications in the pharmaceutical and material science industries.
Building Blocks
Their unique chemical structures make them useful building blocks for the synthesis of more complex organic molecules.
Physical and Chemical Properties
Both compounds exhibit diverse physical and chemical properties, making them valuable tools for researchers and synthetic chemists.
Reactivity
The presence of electron-withdrawing fluorine atoms and electron-donating methoxy groups in both compounds can influence their reactivity in various chemical reactions.
Solubility
Due to the presence of polar functional groups (fluorine and methoxy groups), both compounds are likely to be soluble in polar solvents like water and alcohols.
Stability
The aromatic nature of both compounds contributes to their stability, as the delocalized pi electrons in the benzene and toluene rings provide resistance to reactions that would break the ring.
Synthesis
Both compounds can be synthesized through various organic reactions, such as electrophilic substitution, nucleophilic substitution, or free radical reactions, depending on the specific starting materials and desired product.
Check Digit Verification of cas no
The CAS Registry Mumber 90470-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,7 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 90470-67:
(7*9)+(6*0)+(5*4)+(4*7)+(3*0)+(2*6)+(1*7)=130
130 % 10 = 0
So 90470-67-0 is a valid CAS Registry Number.
90470-67-0Relevant articles and documents
Photochemical synthesis of acetals utilizing Schreiner's thiourea as the catalyst
Kokotos, Christoforos G.,Nikitas, Nikolaos F.,Spiliopoulou, Nikoleta
supporting information, p. 3539 - 3545 (2020/06/25)
Acetalization of aldehydes is an area of great importance in Organic Chemistry for both synthetic and biological puproses. Herein, we report a mild, inexpensive and green photochemical protocol, where Schreiner's thiourea (N,N′-bis[3,5-bis(trifluoromethyl)-phenyl]-thiourea) is utilized as the catalyst and cheap household lamps as the light source. A variety of aromatic and aliphatic aldehydes were converted into acetals in good to high yields (23 examples, 36-96% yield) and an example of the synthesis of a cyclic acetal is provided. The reaction mechanism was also studied.
Silver-Catalyzed Olefination of Acetals and Ketals with Diazoesters to β-Alkoxyacrylates
Li, Jiawen,Qian, Bo,Huang, Hanmin
supporting information, p. 7090 - 7094 (2018/11/23)
The first silver-catalyzed reaction of acetals or ketals with diazoesters leading to trisubstituted or tetrasubstituted β-alkoxyacrylates is now reported. A broad range of acetals and ketals bearing different substituents is compatible with this protocol and thus provides an attractive approach for the synthesis of complex β-alkoxyacrylates. The power of this method was further demonstrated by the successful synthesis of picoxystrobin, which is one of the most popular agricultural fungicides commercialized by Dupont.
Stepwise construction of discrete heterometallic coordination cages based on self-sorting strategy
Li, Hao,Han, Ying-Feng,Lin, Yue-Jian,Guo, Zi-Wei,Jin, Guo-Xin
supporting information, p. 2982 - 2985 (2014/03/21)
A chelation-directed self-sorting synthesis of a series of cationic heterometallic coordination cages (HCCs) with tunable sizes is described. Two complexation modes were found in the cage-forming process. Metal-anchoring host-guest behavior and size-selective in-cage catalytic activities were found for the HCCs.
