132431-12-0 Usage
Chemical Structure
苯基环连接一个2,3-二氢吲哚环，并通过酯基连接一个苄基 2,3-Dihydro-indole-1-carboxylic acid benzyl ester的化学结构由一个苯基环和一个2,3-二氢吲哚环组成，并通过酯基连接一个苄基。
Derivative of 2,3-Dihydro-Indole-1-Carboxylic Acid
2,3-Dihydro-indole-1-carboxylic acid benzyl ester是2,3-二氢吲哚-1-羧酸的苄酯衍生物。
Biological Activity
2,3-Dihydro-indole-1-carboxylic acid benzyl ester is a key intermediate in the synthesis of various biologically active molecules and pharmaceuticals. 2,3-二氢吲哚-1-羧酸苄酯是合成各种生物活性分子和药物的关键中间体。
Potential Use as a Starting Material
2,3-Dihydro-indole-1-carboxylic acid benzyl ester has the potential to be used as a starting material for the production of pharmaceutical drugs and other chemical products. 2,3-二氢吲哚-1-羧酸苄酯有可能用作生产药物和其他化学产品的起始材料。
Building Block in Organic Chemistry
2,3-Dihydro-indole-1-carboxylic acid benzyl ester is an important building block in organic chemistry. 2,3-二氢吲哚-1-羧酸苄酯是有机化学中的重要构建模块。
Synthesis of Heterocyclic Compounds
2,3-Dihydro-indole-1-carboxylic acid benzyl ester can be used in the synthesis of various heterocyclic compounds with potential biological activities. 2,3-二氢吲哚-1-羧酸苄酯可用于合成具有潜在生物活性的各种杂环化合物。
Applications in Medicinal Chemistry
2,3-Dihydro-indole-1-carboxylic acid benzyl ester may have potential applications in the field of medicinal chemistry and drug discovery. 2,3-二氢吲哚-1-羧酸苄酯在药物化学和药物发现领域可能有潜在应用。
Check Digit Verification of cas no
The CAS Registry Mumber 132431-12-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,3 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 132431-12:
(8*1)+(7*3)+(6*2)+(5*4)+(4*3)+(3*1)+(2*1)+(1*2)=80
80 % 10 = 0
So 132431-12-0 is a valid CAS Registry Number.
132431-12-0Relevant articles and documents
Gold-Catalyzed Friedel–Crafts-Like Reaction of Benzylic Alcohols to Afford 1,1-Diarylalkanes
Oakley, James V.,Stanley, Tyler J.,Jesse, Kate A.,Melanese, Amanda K.,Alvarez, Araceli A.,Prince, Aloha L.,Cain, Stephanie E.,Wenzel, Anna G.,Iafe, Robert G.
, p. 7063 - 7066 (2019)
A gold-catalyzed, Friedel–Crafts-like benzylation of unactivated benzylic alcohols to form 1,1-diarylalkanes has been developed. The operationally convenient method uses only 1.3 equivalents of the electron-rich arene, employs readily available starting m
INHIBITION OF BACTERIAL BIOFILMS WITH ARYL CARBAMATES
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Page/Page column 33, (2012/02/01)
Disclosure is provided for carbamate compounds that prevent, remove and/or inhibit the formation of biofilms, compositions including these compounds, devices including these compounds, and methods of using the same.
Nickel-mediated inter- and intramolecular reductive cross-coupling of unactivated alkyl bromides and aryl iodides at room temperature
Yan, Chang-Song,Peng, Yu,Xu, Xiao-Bo,Wang, Ya-Wen
, p. 6039 - 6048 (2012/06/18)
A nickel-mediated intermolecular reductive cross-coupling reaction of unactivated alkyl bromides and aryl iodides at room temperature has been developed and successfully extended to less explored intramolecular versions and tandem cyclization-intermolecular cross-coupling. Highly stereoselective (or stereospecific) synthesis of linear-fused perhydrofuro[2,3-b]furan (pyran) and spiroketal skeletons allows rapid access to these useful building blocks, which would be potentially valuable in the synthesis of relevant natural products. A rational explanation for the formation of contiguous stereogenic centers is given. Copyright
