155062-48-9 Usage
Chemical family
Belongs to the oxadiazole family, which is a group of five-membered heterocyclic compounds containing two nitrogen atoms and one oxygen atom.
Structure
A carbonyl chloride derivative with a methyl group attached to the 5th carbon atom.
Potential applications
Has potential applications in the field of organic synthesis and pharmaceuticals due to its unique structure and reactivity.
Building block
Can be used as a building block for the synthesis of various organic compounds and pharmaceutical drugs.
Reagent
May have potential use as a reagent in chemical reactions.
Precursor
Can serve as a precursor for the development of new materials.
Further research
Its specific uses and applications would depend on further research and development in the field.
Molecular weight
Approximately 156.54 g/mol (calculated from the chemical formula)
Appearance
The appearance of the compound is not provided in the material, but it is likely a solid or a liquid depending on its stability and purity.
Stability
The stability of the compound is not mentioned in the material, but it is important to consider when working with reactive compounds like carbonyl chlorides.
Safety precautions
The safety precautions and potential hazards associated with handling and using this compound are not provided in the material, but it is crucial to follow proper safety protocols when working with potentially reactive chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 155062-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,0,6 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 155062-48:
(8*1)+(7*5)+(6*5)+(5*0)+(4*6)+(3*2)+(2*4)+(1*8)=119
119 % 10 = 9
So 155062-48-9 is a valid CAS Registry Number.
155062-48-9Relevant articles and documents
The discovery of MK-4256, a potent SSTR3 antagonist as a potential treatment of type 2 diabetes
He, Shuwen,Ye, Zhixiong,Truong, Quang,Shah, Shrenik,Du, Wu,Guo, Liangqin,Dobbelaar, Peter H.,Lai, Zhong,Liu, Jian,Jian, Tianying,Qi, Hongbo,Bakshi, Raman K.,Hong, Qingmei,Dellureficio, James,Pasternak, Alexander,Feng, Zhe,Dejesus, Reynalda,Yang, Lihu,Reibarkh, Mikhail,Bradley, Scott A.,Holmes, Mark A.,Ball, Richard G.,Ruck, Rebecca T.,Huffman, Mark A.,Wong, Frederick,Samuel, Koppara,Reddy, Vijay B.,Mitelman, Stan,Tong, Sharon X.,Chicchi, Gary G.,Tsao, Kwei-Lan,Trusca, Dorina,Wu, Margaret,Shao, Qing,Trujillo, Maria E.,Eiermann, George J.,Li, Cai,Zhang, Bei B.,Howard, Andrew D.,Zhou, Yun-Ping,Nargund, Ravi P.,Hagmann, William K.
supporting information; experimental part, p. 484 - 489 (2012/10/08)
A structure-activity relationship study of the imidazolyl-β- tetrahydrocarboline series identified MK-4256 as a potent, selective SSTR3 antagonist, which demonstrated superior efficacy in a mouse oGTT model. MK-4256 reduced glucose excursion in a dose-dependent fashion with maximal efficacy achieved at doses as low as 0.03 mg/kg po. As compared with glipizide, MK-4256 showed a minimal hypoglycemia risk in mice.
Substituted sulphonyl amino(thio)carbonyl compounds and their use as herbicides
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Page column 53, (2010/11/30)
The invention relates to novel sulfonylamino(thio)carbonyl compounds of the formula (I), in whichn represents the numbers 0, 1 or 2,A represents a single bond, or oxygen or sulfur, or the grouping N—R, in which R represents hydrogen, alkyl, alkenyl, alkin